Homo sapiens cDNA FLJ40898 fis, clone UTERU2003057, highly similar to - Nucleotide

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Expanding Genotype-Phenotype Correlation of CLCNKA and CLCNKB Variants Linked to Hearing Loss. [Int J Mol Sci. 2023]
Expanding Genotype-Phenotype Correlation of CLCNKA and CLCNKB Variants Linked to Hearing Loss.
Yun Y, Park SS, Lee S, Seok H, Park S, Lee SY. Int J Mol Sci. 2023 Dec 3; 24(23). Epub 2023 Dec 3.
Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions. [Genome Med. 2023]
Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions.
Tschernoster N, Erger F, Kohl S, Reusch B, Wenzel A, Walsh S, Thiele H, Becker C, Franitza M, Bartram MP, et al. Genome Med. 2023 Aug 23; 15(1):62. Epub 2023 Aug 23.
A novel CLCNKB variant in a Chinese family with classic Bartter syndrome and prenatal genetic diagnosis. [Mol Genet Genomic Med. 2022]
A novel CLCNKB variant in a Chinese family with classic Bartter syndrome and prenatal genetic diagnosis.
Zhao Q, Xiang Q, Tan Y, Xiao X, Xie H, Wang H, Yang M, Liu S. Mol Genet Genomic Med. 2022 Oct; 10(10):e2027. Epub 2022 Aug 1.

RefSeq alternative splicing
See 2 reference mRNA sequence splice variants for the CLCNKB gene.

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Nucleotide