| Excerpt | Relevance | Reference |
|---|
| "Pseudohypoaldosteronism type 1 (PHA-1) is an inherited disease characterized by severe neonatal salt-wasting and caused by mutations in subunits of the amiloride-sensitive epithelial sodium channel (ENaC)." | 7.69 | A mutation causing pseudohypoaldosteronism type 1 identifies a conserved glycine that is involved in the gating of the epithelial sodium channel. ( Chang, SS; Firsov, D; Gautschi, I; Gründer, S; Jaeger, NF; Lifton, RP; Rossier, BC; Schild, L, 1997) |
| "Pseudohypoaldosteronism type 1 (PHA-1) is an inherited disease characterized by severe neonatal salt-wasting and caused by mutations in subunits of the amiloride-sensitive epithelial sodium channel (ENaC)." | 3.69 | A mutation causing pseudohypoaldosteronism type 1 identifies a conserved glycine that is involved in the gating of the epithelial sodium channel. ( Chang, SS; Firsov, D; Gautschi, I; Gründer, S; Jaeger, NF; Lifton, RP; Rossier, BC; Schild, L, 1997) |