Varaico: Literature-Extracted Genetic Variants

Gene:GRXCR2
Variant:p.K22R
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GRXCR2

NM_001080516.2:p.K22R

Associated Papers

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

Wonkam A et al.

Molecular Genetics & Genomic Medicine, 2021

Clinical and genetic study of 12 Chinese Han families with nonsyndromic deafness.

Wu D et al.

Molecular Genetics & Genomic Medicine, 2020

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."