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Whole exome sequencing reveals a biallelic frameshift mutation in GRXCR2 in hearing impairment in Cameroon

Ambroise Wonkam1,2, Kamogelo Lebeko1, Shaheen Mowla3

  • 1Department of Medicine, Division of Human Genetics, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.

Molecular Genetics & Genomic Medicine
|February 2, 2021
PubMed
Abstract

Keywords:
GRXCR2AfricaCameroonhearing impairmentwhole exome sequencing

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