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KDM5A mutations identified in autism spectrum disorder using forward genetics.
El Hayek, Lauretta; Tuncay, Islam Oguz; Nijem, Nadine; Russell, Jamie; Ludwig, Sara; Kaur, Kiran; Li, Xiaohong; Anderton, Priscilla; Tang, Miao; Gerard, Amanda; Heinze, Anja; Zacher, Pia; Alsaif, Hessa S; Rad, Aboulfazl; Hassanpour, Kazem; Abbaszadegan, Mohammad Reza; Washington, Camerun; DuPont, Barbara R; Louie, Raymond J; Couse, Madeline; Faden, Maha; Rogers, R Curtis; Abou Jamra, Rami; Elias, Ellen R; Maroofian, Reza; Houlden, Henry; Lehman, Anna; Beutler, Bruce; Chahrour, Maria H.
Afiliação
  • El Hayek L; Eugene McDermott Center for Human Growth and Development, University of Texas Southwestern Medical Center, Dallas, United States.
  • Tuncay IO; Department of Neuroscience, University of Texas Southwestern Medical Center, Dallas, United States.
  • Nijem N; Eugene McDermott Center for Human Growth and Development, University of Texas Southwestern Medical Center, Dallas, United States.
  • Russell J; Center for the Genetics of Host Defense, University of Texas Southwestern Medical Center, Dallas, United States.
  • Ludwig S; Center for the Genetics of Host Defense, University of Texas Southwestern Medical Center, Dallas, United States.
  • Kaur K; Eugene McDermott Center for Human Growth and Development, University of Texas Southwestern Medical Center, Dallas, United States.
  • Li X; Center for the Genetics of Host Defense, University of Texas Southwestern Medical Center, Dallas, United States.
  • Anderton P; Center for the Genetics of Host Defense, University of Texas Southwestern Medical Center, Dallas, United States.
  • Tang M; Center for the Genetics of Host Defense, University of Texas Southwestern Medical Center, Dallas, United States.
  • Gerard A; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, United States.
  • Heinze A; Texas Children's Hospital, Houston, United States.
  • Zacher P; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.
  • Alsaif HS; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.
  • Rad A; The Saxon Epilepsy Center Kleinwachau, Radeberg, Germany.
  • Hassanpour K; Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
  • Abbaszadegan MR; Cellular and Molecular Research Center, Sabzevar University of Medical Sciences, Sabzevar, Islamic Republic of Iran.
  • Washington C; Non-Communicable Diseases Research Center, Sabzevar University of Medical Sciences, Sabzevar, Islamic Republic of Iran.
  • DuPont BR; Pardis Clinical and Genetics Laboratory, Mashhad, Islamic Republic of Iran.
  • Louie RJ; Division of Human Genetics, Avicenna Research Institute, Mashhad University of Medical Sciences, Mashhad, Islamic Republic of Iran.
  • Couse M; Greenwood Genetic Center, Greenwood, United States.
  • Faden M; Greenwood Genetic Center, Greenwood, United States.
  • Rogers RC; Department of Medical Genetics, University of British Columbia, British Columbia Children's and Women's Hospital Research Institute, Vancouver, Canada.
  • Abou Jamra R; Department of Medical Genetics, University of British Columbia, British Columbia Children's and Women's Hospital Research Institute, Vancouver, Canada.
  • Elias ER; Department of Genetics, King Saud Medical City, Riyadh, Saudi Arabia.
  • Maroofian R; Greenwood Genetic Center, Greenwood, United States.
  • Houlden H; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.
  • Lehman A; Department of Pediatrics and Genetics, University of Colorado School of Medicine, Aurora, United States.
  • Beutler B; Department of Neuromuscular Diseases, University College London, Queen Square Institute of Neurology, London, United Kingdom.
  • Chahrour MH; Department of Neuromuscular Diseases, University College London, Queen Square Institute of Neurology, London, United Kingdom.
Elife ; 92020 12 22.
Article em En | MEDLINE | ID: mdl-33350388
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteína 2 de Ligação ao Retinoblastoma / Transtorno do Espectro Autista Tipo de estudo: Prognostic_studies Limite: Adolescent / Animals / Child, preschool / Female / Humans / Male Idioma: En Revista: Elife Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
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Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteína 2 de Ligação ao Retinoblastoma / Transtorno do Espectro Autista Tipo de estudo: Prognostic_studies Limite: Adolescent / Animals / Child, preschool / Female / Humans / Male Idioma: En Revista: Elife Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos