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G130V de novo mutation in an Iranian pedigree with nonsyndromic hearing loss without palmoplantar keratoderma.
Babanejad, Mojgan; Zarandy, Masoud Motasaddi; Nikzat, Nooshin; Bazazzadegan, Niloofar; Arzhangi, Sanaz; Mohseni, Marzieh; Kahrizi, Kimia; Najmabadi, Hossein.
Afiliación
  • Babanejad M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Zarandy MM; Cochlear Implant Center and Department of Otorhinolaryngology, Amir Aalam Hospital, Tehran University of Medical Sciences, Tehran, Iran.
  • Nikzat N; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Bazazzadegan N; 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.
  • Mohseni M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, 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. Electronic address: hnajm12@yahoo.com.
Int J Pediatr Otorhinolaryngol ; 126: 109607, 2019 Nov.
Article en En | MEDLINE | ID: mdl-31419744
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Conexinas / Pérdida Auditiva Sensorineural / Mutación Límite: Adolescent / Female / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Int J Pediatr Otorhinolaryngol Año: 2019 Tipo del documento: Article País de afiliación: Irán
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Conexinas / Pérdida Auditiva Sensorineural / Mutación Límite: Adolescent / Female / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Int J Pediatr Otorhinolaryngol Año: 2019 Tipo del documento: Article País de afiliación: Irán