Prediction and interpretation of rare missense variant in OTOG associated with hearing loss.

Askari, Masomeh; Moradi, Zahra; Mohammadi, Mahsa; Lagzian, Milad; Asgharzade, Samira

Askari, Masomeh; Moradi, Zahra; Mohammadi, Mahsa; Lagzian, Milad; Asgharzade, Samira.

Afiliação

Askari M; Basic and Molecular Epidemiology of Gastrointestinal Disorders Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Moradi Z; Cellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran.
Mohammadi M; Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran; Department of Stem Cells and developmental biology, University of Science and Culture, ACECR, Tehran, Iran.
Lagzian M; Department of Biology, University of Sistan and Baluchestan, Zahedan, Iran. Electronic address: m.lagzian@science.usb.ac.ir.
Asgharzade S; Cellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran. Electronic address: Asgharzade.s@skums.ac.ir.

Genomics ; 113(4): 2793-2799, 2021 07.

Article em En | MEDLINE | ID: mdl-34118384

Assuntos

Surdez; Perda Auditiva; Surdez/genética; Perda Auditiva/genética; Homozigoto; Humanos; Irã (Geográfico); Glicoproteínas de Membrana/genética; Mutação; Mutação de Sentido Incorreto; Linhagem; Sequenciamento do Exoma/métodos

Palavras-chave

Homozygous OTOG; Inherited non-syndromic hearing loss; Molecular diagnosis; Next-generation sequencing; Protein modeling

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Surdez / Perda Auditiva Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans País/Região como assunto: Asia Idioma: En Revista: Genomics Assunto da revista: GENETICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Irã País de publicação: Estados Unidos

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