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Volumn 79, Issue 3, 1994, Pages 407-414
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Liddle's syndrome: Heritable human hypertension caused by mutations in the β subunit of the epithelial sodium channel
a b a a a c d e f g h h a |
Author keywords
[No Author keywords available]
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Indexed keywords
ALDOSTERONE;
AMILORIDE;
AMINO ACID;
CYTOSINE;
DNA;
MINERALOCORTICOID;
PEPTIDE;
POTASSIUM;
PROTEIN;
SODIUM;
SODIUM CHANNEL;
SPIRONOLACTONE;
TRIAMTERENE;
ARTICLE;
BETA CHAIN;
BLOOD PRESSURE;
CARBOXY TERMINAL SEQUENCE;
CHROMOSOME 16;
CLINICAL ARTICLE;
DNA SEQUENCE;
FRAMESHIFT MUTATION;
GENE;
GENE MAPPING;
GENE MUTATION;
GENETIC POLYMORPHISM;
GENOTYPE;
HEREDITARY HYPERTENSION;
HUMAN;
HYPOKALEMIA;
KIDNEY EPITHELIUM;
LIDDLE SYNDROME;
NONHUMAN;
NUCLEIC ACID BASE SUBSTITUTION;
POLYACRYLAMIDE GEL ELECTROPHORESIS;
POLYMERASE CHAIN REACTION;
PRIORITY JOURNAL;
SEQUENCE HOMOLOGY;
STOP CODON;
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EID: 0027946089
PISSN: 00928674
EISSN: None
Source Type: Journal
DOI: 10.1016/0092-8674(94)90250-X Document Type: Article |
Times cited : (1215)
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References (29)
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