Gene: [16p12/SCNN1G] sodium channel, nonvoltage-gated 1 gamma; pseudohypoaldosteronism, type I (autosomal recessive; persian-jewish type; SCNN1G deficiency; MIM:264350); pseudoaldosteronism (Liddle syndrome; SCNN1G deficiency; MIM:177200);
REF | MUT
"Hansson JH &: Nature Genet, 11, N1, 76-82, 1995 PAT,MUT "Strautnieks SS &: Nature Genet, 13, N2, 248-250, 1996 CLO,SEQ,LOC "Voilley N &: Genomics, 28, 560-565, 1995 |
SWI | SWISSPROT: P51170 |
KEY | neu, sign, mem, myo, ion |
CLA | coding, basic |
LOC | 16 p12.2-.1 |
MIM | MIM: 600761 |
