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Article

Whole-exome sequencing reveals known and candidate genes for hearing impairment in Mali.

HGG advances - 9 Jan 2025

Yalcouyé Abdoulaye, Schrauwen Isabelle, Traoré Oumou, Bamba Salia, Aboagye Elvis Twumasi, Acharya Anushree, Bharadwaj Thashi, Latanich Rachel, Esoh Kevin, Fortes-Lima Cesar A, de Kock Carmen, Jonas Mario, Maiga Alassane Dit Baneye, Cissé Cheick A K, Sangaré Moussa A, Guinto Cheick O, Landouré Guida, Leal Suzanne M, Wonkam Ambroise

Abstract excerpt

Hearing impairment (HI) is the most common neurosensory disorder globally and is reported to be more prevalent in low-income countries. In high-income countries, up to 50% of congenital childhood HI is of genetic origin. However, there are limited genetic data on HI from sub-Saharan African populations. In this study, we investigated the genetic causes of HI in the Malian populations, using whole-exome...

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Source

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Identifiers

PMID: 39663698
DOI: 10.1016/j.xhgg.2024.100391
PMCID: PMC11730241

Genes

UBFD1
CDH23
CIB2
EYA1
GAS2
GJB2
MYO15A
MYO7A
OTOGL
PJVK
SLC26A4
TMC1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

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