Your browser doesn't support javascript.
loading
Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.
Jin, Sheng Chih; Lewis, Sara A; Bakhtiari, Somayeh; Zeng, Xue; Sierant, Michael C; Shetty, Sheetal; Nordlie, Sandra M; Elie, Aureliane; Corbett, Mark A; Norton, Bethany Y; van Eyk, Clare L; Haider, Shozeb; Guida, Brandon S; Magee, Helen; Liu, James; Pastore, Stephen; Vincent, John B; Brunstrom-Hernandez, Janice; Papavasileiou, Antigone; Fahey, Michael C; Berry, Jesia G; Harper, Kelly; Zhou, Chongchen; Zhang, Junhui; Li, Boyang; Zhao, Hongyu; Heim, Jennifer; Webber, Dani L; Frank, Mahalia S B; Xia, Lei; Xu, Yiran; Zhu, Dengna; Zhang, Bohao; Sheth, Amar H; Knight, James R; Castaldi, Christopher; Tikhonova, Irina R; López-Giráldez, Francesc; Keren, Boris; Whalen, Sandra; Buratti, Julien; Doummar, Diane; Cho, Megan; Retterer, Kyle; Millan, Francisca; Wang, Yangong; Waugh, Jeff L; Rodan, Lance; Cohen, Julie S; Fatemi, Ali.
Afiliação
  • Jin SC; Department of Genetics, Yale University School of Medicine, New Haven, CT, USA.
  • Lewis SA; Laboratory of Human Genetics and Genomics, Rockefeller University, New York, NY, USA.
  • Bakhtiari S; Department of Genetics, Washington University School of Medicine, St Louis, MO, USA.
  • Zeng X; Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA.
  • Sierant MC; Departments of Child Health, Neurology, and Cellular & Molecular Medicine, and Program in Genetics, University of Arizona College of Medicine-Phoenix, Phoenix, AZ, USA.
  • Shetty S; Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA.
  • Nordlie SM; Departments of Child Health, Neurology, and Cellular & Molecular Medicine, and Program in Genetics, University of Arizona College of Medicine-Phoenix, Phoenix, AZ, USA.
  • Elie A; Department of Genetics, Yale University School of Medicine, New Haven, CT, USA.
  • Corbett MA; Laboratory of Human Genetics and Genomics, Rockefeller University, New York, NY, USA.
  • Norton BY; Department of Genetics, Yale University School of Medicine, New Haven, CT, USA.
  • van Eyk CL; Laboratory of Human Genetics and Genomics, Rockefeller University, New York, NY, USA.
  • Haider S; Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA.
  • Guida BS; Departments of Child Health, Neurology, and Cellular & Molecular Medicine, and Program in Genetics, University of Arizona College of Medicine-Phoenix, Phoenix, AZ, USA.
  • Magee H; Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA.
  • Liu J; Departments of Child Health, Neurology, and Cellular & Molecular Medicine, and Program in Genetics, University of Arizona College of Medicine-Phoenix, Phoenix, AZ, USA.
  • Pastore S; Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA.
  • Vincent JB; Departments of Child Health, Neurology, and Cellular & Molecular Medicine, and Program in Genetics, University of Arizona College of Medicine-Phoenix, Phoenix, AZ, USA.
  • Brunstrom-Hernandez J; Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia.
  • Papavasileiou A; Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA.
  • Fahey MC; Departments of Child Health, Neurology, and Cellular & Molecular Medicine, and Program in Genetics, University of Arizona College of Medicine-Phoenix, Phoenix, AZ, USA.
  • Berry JG; Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia.
  • Harper K; Department of Pharmaceutical and Biological Chemistry, UCL School of Pharmacy, London, UK.
  • Zhou C; Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA.
  • Zhang J; Departments of Child Health, Neurology, and Cellular & Molecular Medicine, and Program in Genetics, University of Arizona College of Medicine-Phoenix, Phoenix, AZ, USA.
  • Li B; Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA.
  • Zhao H; Departments of Child Health, Neurology, and Cellular & Molecular Medicine, and Program in Genetics, University of Arizona College of Medicine-Phoenix, Phoenix, AZ, USA.
  • Heim J; Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA.
  • Webber DL; Departments of Child Health, Neurology, and Cellular & Molecular Medicine, and Program in Genetics, University of Arizona College of Medicine-Phoenix, Phoenix, AZ, USA.
  • Frank MSB; Molecular Brain Sciences, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.
  • Xia L; Molecular Brain Sciences, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.
  • Xu Y; One CP Place, Plano, TX, USA.
  • Zhu D; Division of Paediatric Neurology, Iaso Children's Hospital, Athens, Greece.
  • Zhang B; Department of Pediatrics, Monash University, Melbourne, Victoria, Australia.
  • Sheth AH; Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia.
  • Knight JR; Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia.
  • Castaldi C; Henan Key Laboratory of Child Genetics and Metabolism, Rehabilitation Department, Children's Hospital of Zhengzhou University, Zhengzhou, China.
  • Tikhonova IR; Department of Genetics, Yale University School of Medicine, New Haven, CT, USA.
  • López-Giráldez F; Department of Biostatistics, Yale School of Public Health, New Haven, CT, USA.
  • Keren B; Department of Biostatistics, Yale School of Public Health, New Haven, CT, USA.
  • Whalen S; Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA.
  • Buratti J; Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia.
  • Doummar D; Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia.
  • Cho M; Henan Key Laboratory of Child Brain Injury, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
  • Retterer K; Henan Key Laboratory of Child Brain Injury, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
  • Millan F; Henan Key Laboratory of Child Brain Injury, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
  • Wang Y; Henan Key Laboratory of Child Brain Injury, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
  • Waugh JL; Department of Genetics, Yale University School of Medicine, New Haven, CT, USA.
  • Rodan L; Yale Center for Genome Analysis, Yale University, New Haven, CT, USA.
  • Cohen JS; Yale Center for Genome Analysis, Yale University, New Haven, CT, USA.
  • Fatemi A; Yale Center for Genome Analysis, Yale University, New Haven, CT, USA.
Nat Genet ; 53(3): 412, 2021 Mar.
Article em En | MEDLINE | ID: mdl-33432185
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Risk_factors_studies Idioma: En Revista: Nat Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Risk_factors_studies Idioma: En Revista: Nat Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos