From: Complicated Gitelman syndrome and autoimmune thyroid disease: a case report with a new homozygous mutation in the SLC12A3 gene and literature review
SLC12A3
SCN4A
KCNJ2
SLC12A1
HSD11B2
ATP6V0A4
KCNJ1
KCNJ5
KCNJ10
CLCNKB
SCCN1B-exon13
SLC34A1
BSND
SCCN1G-exon13
EHHADH
CLCNKA
CYP11B1
HNF4A
CASR
CTP17A1
SLC4A1
CACNA1S
NR3C1
KCNE3
CACNA1D