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.