Homo sapiens cadherin related family member 1 (CDHR1), RefSeqGene on c - Nucleotide

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CDHR1-Related Cone-Rod Dystrophy: Clinical Characteristics, Imaging Findings, and Genetic Test Results-A Case Report. [Medicina (Kaunas). 2023]
CDHR1-Related Cone-Rod Dystrophy: Clinical Characteristics, Imaging Findings, and Genetic Test Results-A Case Report.
Sobolewska M, Świerczyńska M, Dorecka M, Wyględowska-Promieńska D, Krawczyński MR, Mrukwa-Kominek E. Medicina (Kaunas). 2023 Feb 17; 59(2). Epub 2023 Feb 17.
Clinical Phenotypes of CDHR1-Associated Retinal Dystrophies. [Genes (Basel). 2022]
Clinical Phenotypes of CDHR1-Associated Retinal Dystrophies.
Malechka VV, Cukras CA, Chew EY, Sergeev YV, Blain D, Jeffrey BG, Ullah E, Hufnagel RB, Brooks BP, Huryn LA, et al. Genes (Basel). 2022 May 22; 13(5). Epub 2022 May 22.
Novel mutations in PDE6A and CDHR1 cause retinitis pigmentosa in Pakistani families. [Int J Ophthalmol. 2021]
Novel mutations in PDE6A and CDHR1 cause retinitis pigmentosa in Pakistani families.
Dawood M, Lin S, Din TU, Shah IU, Khan N, Jan A, Marwan M, Sultan K, Nowshid M, Tahir R, et al. Int J Ophthalmol. 2021; 14(12):1843-1851. Epub 2021 Dec 18.

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Nucleotide