QuickView for CLCNKB;jsessionid=7EF0FBD10813AABF5D059B5F4A1F873E (gene)

1. Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions.
2. Impairment in renal medulla development underlies salt wasting in Clc-k2 channel deficiency.
3. Thirteen novel CLCNKB variants and genotype/phenotype association study in 42 Chinese patients with …
4. Two novel mutations in the CLCNKB gene leading to classic Bartter syndrome presenting as syncope and…
5. Simultaneous Homozygous Mutations in SLC12A3 and CLCNKB in an Inbred Chinese Pedigree.

There were no clinical trials for CLCNKB;jsessionid=7EF0FBD10813AABF5D059B5F4A1F873E