Whole-Exome Sequencing Reveals a Rare Variant of <i>OTOF</i> Gene Causing Congenital Non-syndromic Hearing Loss Among Large Muslim Families Favoring Consanguinity.

Fareed, Mohd; Sharma, Varun; Singh, Inderpal; Rehman, Sayeed Ur; Singh, Gurdarshan; Afzal, Mohammad

Whole-Exome Sequencing Reveals a Rare Variant of OTOF Gene Causing Congenital Non-syndromic Hearing Loss Among Large Muslim Families Favoring Consanguinity.

Fareed, Mohd; Sharma, Varun; Singh, Inderpal; Rehman, Sayeed Ur; Singh, Gurdarshan; Afzal, Mohammad.

Afiliação

Fareed M; PK-PD Formulation and Toxicology Division, CSIR Indian Institute of Integrative Medicine, Jammu, India.
Sharma V; Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, India.
Singh I; Ancient DNA Laboratory, Birbal Sahni Institute of Palaeosciences, Lucknow, Uttar Pradesh, India.
Rehman SU; BioinfoRes, Jammu, India.
Singh G; Department of Biochemistry, School of Chemical and Life Sciences, Jamia Hamdard, New Delhi, India.
Afzal M; PK-PD Formulation and Toxicology Division, CSIR Indian Institute of Integrative Medicine, Jammu, India.

Front Genet ; 12: 641925, 2021.

Article em En | MEDLINE | ID: mdl-34113375

Palavras-chave

Indian population; Jammu and Kashmir (J and K); autosomal recessive (AR) diseases; cousin marriages; deaf mutes; genetic counseling; hearing disorders; hearing impairment

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Revista: Front Genet Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Índia

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