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IFT27, encoding a small GTPase component of IFT particles, is mutated in a consanguineous family with Bardet-Biedl syndrome.
Aldahmesh, Mohammed A; Li, Yuanyuan; Alhashem, Amal; Anazi, Shams; Alkuraya, Hisham; Hashem, Mais; Awaji, Ali A; Sogaty, Sameera; Alkharashi, Abdullah; Alzahrani, Saeed; Al Hazzaa, Selwa A; Xiong, Yong; Kong, Shanshan; Sun, Zhaoxia; Alkuraya, Fowzan S.
Afiliação
  • Aldahmesh MA; Department of Genetics and.
  • Li Y; Department of Genetics and.
  • Alhashem A; Deparment of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.
  • Anazi S; Department of Genetics and.
  • Alkuraya H; Department of Ophthalmology, College of Medicine, Imam Muhammad Ibn Saud Islamic University, Riyadh, Saudi Arabia.
  • Hashem M; Department of Genetics and.
  • Awaji AA; Department of Pediatrics, King Fahad Central Hospital, Jazan, Saudi Arabia.
  • Sogaty S; Department of Medical Genetics, King Fahad General Hospital, Jeddah, Saudi Arabia and.
  • Alkharashi A; Deparment of Ophthalmology, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
  • Alzahrani S; Department of Pediatric Nephrology, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
  • Al Hazzaa SA; Department of Ophthalmology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia Department of Ophthalmology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.
  • Xiong Y; Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT, USA.
  • Kong S; Department of Genetics and.
  • Sun Z; Department of Genetics and falkuraya@kfshrc.edu.sa zhaoxia.sun@yale.edu.
  • Alkuraya FS; Department of Genetics and Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia falkuraya@kfshrc.edu.sa zhaoxia.sun@yale.edu.
Hum Mol Genet ; 23(12): 3307-15, 2014 Jun 15.
Article em En | MEDLINE | ID: mdl-24488770
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Consanguinidade / Síndrome de Bardet-Biedl / Proteínas Monoméricas de Ligação ao GTP Limite: Adolescent / Animals / Female / Humans / Male País como assunto: Asia Idioma: En Ano de publicação: 2014 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Consanguinidade / Síndrome de Bardet-Biedl / Proteínas Monoméricas de Ligação ao GTP Limite: Adolescent / Animals / Female / Humans / Male País como assunto: Asia Idioma: En Ano de publicação: 2014 Tipo de documento: Article