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

MLA

Mohd Fareed, et al. “Whole-Exome Sequencing Reveals a Rare Variant of OTOF Gene Causing Congenital Non-Syndromic Hearing Loss Among Large Muslim Families Favoring Consanguinity.” Frontiers in Genetics, vol. 12, May 2021. EBSCOhost, https://doi.org/10.3389/fgene.2021.641925.

APA

Mohd Fareed, Varun Sharma, Inderpal Singh, Sayeed Ur Rehman, Gurdarshan Singh, & Mohammad Afzal. (2021). Whole-Exome Sequencing Reveals a Rare Variant of OTOF Gene Causing Congenital Non-syndromic Hearing Loss Among Large Muslim Families Favoring Consanguinity. Frontiers in Genetics, 12. https://doi.org/10.3389/fgene.2021.641925

Chicago

Mohd Fareed, Varun Sharma, Inderpal Singh, Sayeed Ur Rehman, Gurdarshan Singh, and Mohammad Afzal. 2021. “Whole-Exome Sequencing Reveals a Rare Variant of OTOF Gene Causing Congenital Non-Syndromic Hearing Loss Among Large Muslim Families Favoring Consanguinity.” Frontiers in Genetics 12 (May). doi:10.3389/fgene.2021.641925.