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Gitelman Syndrome — Gene Therapy & Clinical Trials | FollowGene
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Gitelman Syndrome
Gitelman Syndrome
Prevalence:
1/40000
renal
Official
·
OMIM:263800
Official
·
ORPHA358
Tubulopathy and hypokalemia due to SLC12A3 gene mutations.
Associated Genes
SLC12A3
Solute Carrier Family 12 Member 3
Chromosome 16
Autosomal Recessive