Open AccessIdentification of homozygous missense variant in SIX5 gene underlying recessive nonsyndromic hearing impairment
Author(s) -
Mohib Ullah Kakar,
Muhammad Akram,
Muhammad Zubair Mehboob,
Muhammad Younus,
Muhammad Bilal,
Ahmed Waqas,
Amizir,
Muhammad Shafi,
Muhammad Umair,
Sajjad Ahmad,
Misbahuddin M. Rafeeq
Publication year - 2022
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0268078
Subject(s) - genetics , missense mutation , sanger sequencing , biology , exome sequencing , hearing loss , gene , candidate gene , genetic heterogeneity , exome , mutation , medicine , phenotype , audiology
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