Whole-Exome Sequencing Identifies a Recurrent Small In-Frame Deletion in MYO15A Causing Autosomal Recessive Nonsyndromic Hearing Loss in 3 Iranian Pedigrees.

Background Hearing loss (HL) is the most prevalent and genetically heterogeneous sensory disabilities in humans throughout the world. Methods In this study, we used whole-exome sequencing (WES) to determine the variant causing autosomal recessive nonsyndromic hearing loss (ARNSHL) segregating in 3 s...

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Bibliographic Details

Published in:	Laboratory Medicine Vol. 53; no. 2; pp. 111 - 123
Main Authors:	Nasrniya, Samane, Miar, Paniz, Narrei, Sina, Sepehrnejad, Mahsa, Nilforoush, Mohammad Hussein, Abtahi, Hamidreza, Tabatabaiefar, Mohammad Amin
Format:	pictorial research tables/charts Journal Article
Published:	Oxford University Press / USA Mar2022
Online Access:	View this record in EBSCOhost