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First Report of Familial Juvenile Hyperuricemic Nephropathy (FJHN) in Iran Caused By a Novel De Novo Mutation (E197X) in UMOD.
Malakoutian, Tahereh; Amouzegar, Atefeh; Vali, Farzaneh; Asgari, Mojgan; Behnam, Babak.
Afiliación
  • Malakoutian T; Hasheminejad Kidney Center, Hospital Management Research Center, Iran University of Medical Sciences, Tehran, Iran.
  • Amouzegar A; Hasheminejad Kidney Center, Hospital Management Research Center, Iran University of Medical Sciences, Tehran, Iran.
  • Vali F; Department of Medical Genetics and Molecular Biology, Faculty of Medicine, Iran University of Medical Sciences (IUMS), Tehran, Iran.
  • Asgari M; Hasheminejad Kidney Center, Hospital Management Research Center, Iran University of Medical Sciences, Tehran, Iran.
  • Behnam B; Department of Medical Genetics and Molecular Biology, Faculty of Medicine, Iran University of Medical Sciences (IUMS), Tehran, Iran.
J Mol Genet Med ; 10(2)2016 Jun.
Article en En | MEDLINE | ID: mdl-27489562
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Mol Genet Med Año: 2016 Tipo del documento: Article País de afiliación: Irán Pais de publicación: Reino Unido
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Mol Genet Med Año: 2016 Tipo del documento: Article País de afiliación: Irán Pais de publicación: Reino Unido