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An Extended Iranian Family with Autosomal Dominant Non-syndromic Hearing Loss Associated with A Nonsense Mutation in the DIAPH1 Gene.
Mohseni, Marzieh; Mohammadi, Yusuf; Zare Ashrafi, Farzane; Ghodratpour, Fatemeh; Jalalvand, Khadijeh; Arzhangi, Sanaz; Babanejad, Mojgan; Azizi, Mohammad Hossein; Kahrizi, Kimia; Najmabadi, Hossein.
Afiliación
  • Mohseni M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Mohammadi Y; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Zare Ashrafi F; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Ghodratpour F; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Jalalvand K; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Arzhangi S; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Babanejad M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Azizi MH; Associate Professor of Otolaryngology, Academy of Medical Sciences of IR Iran, Tehran, Iran.
  • Kahrizi K; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Najmabadi H; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
Arch Iran Med ; 26(3): 176-180, 2023 03 01.
Article en En | MEDLINE | ID: mdl-37543941
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Sordera / Pérdida Auditiva Sensorineural Tipo de estudio: Risk_factors_studies País/Región como asunto: Asia Idioma: En Revista: Arch Iran Med Año: 2023 Tipo del documento: Article
Texto completo
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PubMed Links
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Sordera / Pérdida Auditiva Sensorineural Tipo de estudio: Risk_factors_studies País/Región como asunto: Asia Idioma: En Revista: Arch Iran Med Año: 2023 Tipo del documento: Article