Condition: Pseudohypoaldosteronism, Type IIc
rs111033591
in
WNK1
gene and
Pseudohypoaldosteronism, Type IIc
PMID 15911806
2005 Two mutations in the HSN2 gene explain the high prevalence of HSAN2 in French Canadians.
PMID 15060842
2004 Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the Study of Canadian Genetic Isolates.