Associated Papers
Twelve exonic variants in the SLC12A1 and CLCNKB genes alter RNA splicing in a minigene assay.
Xin Q et al.
Frontiers in Genetics, 2022
Bartter syndrome and growth hormone deficiency: Three siblings with a novel CLCNKB mutation.
Brambilla I et al.
Pediatrics International : Official Journal of the Japan Pediatric Society, 2019
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