Identification of homozygous missense variant in SIX5 gene underlying recessive nonsyndromic hearing impairment.

Identification of homozygous missense variant in SIX5 gene underlying recessive nonsyndromic hearing impairment.

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Hearing impairment (HI) is a heterogeneous condition that affects many individuals globally with different age groups. HI is a genetically and phenotypically heterogeneous disorder. Over the last several years, many genes/loci causing rare autosomal recessive and dominant forms of hearing impairment...

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Bibliographic Details
Main Authors: Mohib Ullah Kakar, Muhammad Akram, Muhammad Zubair Mehboob, Muhammad Younus, Muhammad Bilal, Ahmed Waqas, Amina Nazir, Muhammad Shafi, Muhammad Umair, Sajjad Ahmad, Misbahuddin M Rafeeq
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2022-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0268078

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https://doi.org/10.1371/journal.pone.0268078

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