cadherin-like 23, isoform CRA_a [Homo sapiens]

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CDH23-Associated Usher Syndrome: Clinical Features, Retinal Imaging, and Natural History. [Invest Ophthalmol Vis Sci. 2024]
CDH23-Associated Usher Syndrome: Clinical Features, Retinal Imaging, and Natural History.
de Guimaraes TAC, Robson AG, de Guimaraes IMC, Laich Y, Aychoua N, Wright G, Kalitzeos A, Mahroo OA, Webster AR, Michaelides M. Invest Ophthalmol Vis Sci. 2024 Jul 1; 65(8):27.
A Novel Biallelic Variant in CDH23 Gene in a Family with Atypical USH1D Manifestation: A Literature Review and Investigation of Genotype-Phenotype Correlation. [Audiol Neurootol. 2023]
A Novel Biallelic Variant in CDH23 Gene in a Family with Atypical USH1D Manifestation: A Literature Review and Investigation of Genotype-Phenotype Correlation.
Khorram E, Iravani O, Khorrami M, Amini M, Jahanian S, Nilforoush MH, Mousavi SR, Ehsanifard M, Kheirollahi M. Audiol Neurootol. 2023; 28(4):317-326. Epub 2023 Apr 21.
Association between genetic polymorphisms of cadherin 23 and noise-induced hearing loss: a meta-analysis. [Ann Hum Biol. 2022]
Association between genetic polymorphisms of cadherin 23 and noise-induced hearing loss: a meta-analysis.
Wu ZD, Lu JQ, Du WJ, Wu S. Ann Hum Biol. 2022 Feb; 49(1):41-53.

RefSeq genomic sequence
See the genomic reference sequence for the CDH23 gene (NG_008835.1).
RefSeq protein isoforms
See 9 reference sequence protein isoforms for the CDH23 gene.

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