TY  - GEN
AU  - Simon,D B
AU  - Karet,F E
AU  - Rodriguez-Soriano,J
AU  - Hamdan,J H
AU  - DiPietro,A
AU  - Trachtman,H
AU  - Sanjad,S A
AU  - Lifton,R P
TI  - Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK
SN  - 1061-4036
PY  - 1996///1112
KW  - Amino Acid Sequence
KW  - Bartter Syndrome
KW  - genetics
KW  - Carrier Proteins
KW  - Cell Membrane
KW  - chemistry
KW  - Consanguinity
KW  - Conserved Sequence
KW  - DNA Mutational Analysis
KW  - Female
KW  - Genetic Heterogeneity
KW  - Genotype
KW  - Humans
KW  - Male
KW  - Mutation
KW  - Pedigree
KW  - Polymorphism, Single-Stranded Conformational
KW  - Potassium Channels
KW  - Potassium Channels, Inwardly Rectifying
KW  - Sodium-Potassium-Chloride Symporters
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1038/ng1096-152
ER  -