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
Classification of domains in predicted structures of the human proteome.
Schaeffer RD et al.
Proceedings of the National Academy of Sciences of the United States of America, 2023
36917664 (PubMed )
Supplement: pnas.2214069120.sd02.xlsx › Dataset_S2
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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