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A Novel Cadherin 23 Variant for Hereditary Hearing Loss Reveals Additional Support for a DFNB12 Nonsyndromic Phenotype of CDH23.
Koohiyan, Mahbobeh; Hashemzadeh-Chaleshtori, Morteza; Salehi, Mansoor; Abtahi, Hamidreza; Noori-Daloii, Mohammad Reza; Tabatabaiefar, Mohammad Amin.
Afiliação
  • Koohiyan M; Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
  • Hashemzadeh-Chaleshtori M; Cellular and Molecular Research Center, Basic Health Research Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran.
  • Salehi M; Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
  • Abtahi H; Department of Otolaryngology, Al-Zahra Hospital, Isfahan University of Medical Sciences, Isfahan, Iran.
  • Noori-Daloii MR; Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
  • Tabatabaiefar MA; Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran, tabatabaiefar@med.mui.ac.ir.
Audiol Neurootol ; 25(5): 258-262, 2020.
Article em En | MEDLINE | ID: mdl-32485727
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Caderinas / Perda Auditiva Neurossensorial / Mutação Tipo de estudo: Guideline / Prognostic_studies Limite: Adult / Child / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Caderinas / Perda Auditiva Neurossensorial / Mutação Tipo de estudo: Guideline / Prognostic_studies Limite: Adult / Child / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article