Genotype-phenotype analysis of a newly discovered family with Liddle's syndrome

Journal of Hypertension

Volumn 15, Issue 10, 1997, Pages 1091-1100

  Jeunemaitre, Xavier ^a,c   Bassilana, Frédéric ^b   Persu, Alexandre ^a   Dumont, Cécile ^a   Champigny, Guy ^b   Lazdunski, Michel ^b   Corvol, Pierre ^a   Barbry, Pascal ^b  

^a HÔPITAL BROUSSAIS   (France)

^b INSTITUT DE PHARMACOLOGIE MOLÉCULAIRE ET CELLULAIRE   (France)

^c l'alimentation et l'Environnement   (France)

Author keywords

Aldosterone; Amiloride; Arterial hypertension; Epithelial sodium channel; Genetics; Hypokalemia; Liddle's syndrome; Monogenic disease; Mutations

Indexed keywords

ALDOSTERONE; AMILORIDE; HORMONE; POTASSIUM ION; POTASSIUM SPARING DIURETIC AGENT; PROTEIN SUBUNIT; RENIN; SODIUM CHANNEL;

ADOLESCENT; ADULT; ALDOSTERONE BLOOD LEVEL; ALDOSTERONE URINE LEVEL; ARTICLE; BIOLOGY; BLOOD PRESSURE REGULATION; CARBOXY TERMINAL SEQUENCE; CASE REPORT; CLINICAL FEATURE; DISEASE SEVERITY; DRUG EFFICACY; EXPRESSION VECTOR; FEMALE; FOLLOW UP; GENE DELETION; GENETIC ANALYSIS; GENOTYPE; HUMAN; HYPOKALEMIA; LIDDLE SYNDROME; MALE; MOLECULAR BIOLOGY; ONSET AGE; OPEN READING FRAME; PHENOTYPE; PLASMA RENIN ACTIVITY; POTASSIUM BLOOD LEVEL; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; STOP CODON; XENOPUS;

EID: 0030928166     PISSN: 02636352     EISSN: None     Source Type: Journal    
DOI: 10.1097/00004872-199715100-00007     Document Type: Article

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