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Mutations in Kinesin family member 6 reveal specific role in ependymal cell ciliogenesis and human neurological development.
Konjikusic, Mia J; Yeetong, Patra; Boswell, Curtis W; Lee, Chanjae; Roberson, Elle C; Ittiwut, Rungnapa; Suphapeetiporn, Kanya; Ciruna, Brian; Gurnett, Christina A; Wallingford, John B; Shotelersuk, Vorasuk; Gray, Ryan S.
Afiliação
  • Konjikusic MJ; Department of Pediatrics, Dell Pediatric Research Institute, The University of Texas at Austin, Dell Medical School, Austin, Texas, United States of America.
  • Yeetong P; Department of Molecular Biosciences, Patterson Labs, The University of Texas at Austin, Austin, Texas, United States of America.
  • Boswell CW; Center of Excellence for Medical Genetics, Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
  • Lee C; Excellence Center for Medical Genetics, King Chulalongkorn Memorial Hospital, the Thai Red Cross Society, Bangkok, Thailand.
  • Roberson EC; Division of Human Genetics, Department of Botany, Faculty of Science, Chulalongkorn University, Bangkok, Thailand.
  • Ittiwut R; Program in Developmental & Stem Cell Biology, The Hospital for Sick Children, Toronto, Ontario, Canada; Department of Molecular Genetics, The University of Toronto, Toronto, Ontario, Canada.
  • Suphapeetiporn K; Department of Molecular Biosciences, Patterson Labs, The University of Texas at Austin, Austin, Texas, United States of America.
  • Ciruna B; Department of Molecular Biosciences, Patterson Labs, The University of Texas at Austin, Austin, Texas, United States of America.
  • Gurnett CA; Center of Excellence for Medical Genetics, Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
  • Wallingford JB; Excellence Center for Medical Genetics, King Chulalongkorn Memorial Hospital, the Thai Red Cross Society, Bangkok, Thailand.
  • Shotelersuk V; Center of Excellence for Medical Genetics, Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
  • Gray RS; Excellence Center for Medical Genetics, King Chulalongkorn Memorial Hospital, the Thai Red Cross Society, Bangkok, Thailand.
PLoS Genet ; 14(11): e1007817, 2018 11.
Article em En | MEDLINE | ID: mdl-30475797
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cinesinas / Epêndima / Transtornos do Neurodesenvolvimento / Mutação Tipo de estudo: Prognostic_studies Limite: Animals / Child / Female / Humans / Male Idioma: En Revista: PLoS Genet Assunto da revista: GENETICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cinesinas / Epêndima / Transtornos do Neurodesenvolvimento / Mutação Tipo de estudo: Prognostic_studies Limite: Animals / Child / Female / Humans / Male Idioma: En Revista: PLoS Genet Assunto da revista: GENETICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos