Associated Papers
A Novel Exon 2 Deletion Mutation in the GRXCR1 Gene Associated With Non-Syndromic Hearing Loss: A Case Report and Review of Literatures.
Rastad H et al.
The Annals of Otology, Rhinology, and Laryngology, 2023
Novel mutation in GRXCR1 at DFNB25 lead to progressive hearing loss and dizziness.
Mori K et al.
The Annals of Otology, Rhinology, and Laryngology, 2015
Mutations in Grxcr1 are the basis for inner ear dysfunction in the pirouette mouse.
Odeh H et al.
American Journal of Human Genetics, 2010
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