Title : Clinical characteristics and treatment requirements of children with autosomal recessive pseudohypoaldosteronism.

Pub. Date : 2021 May

PMID : 33690157






1 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Eight children had homozygous mutations in the SCNN1A and SCNN1G genes encoding the epithelial sodium channel subunits alpha and gamma, respectively, including one novel mutation. Sodium sodium channel epithelial 1 subunit gamma Homo sapiens