Mutation analysis of SCNN1B in a family with Liddle's syndrome

Endocrine

Volumn 29, Issue 3, 2006, Pages 385-390

  Wang, Weiqing ^a,b   Zhou, Weiwei ^a   Jiang, Lei ^a   Cui, Bin ^a   Ye, Lei ^a   Su, Tingwei ^a   Wang, Jiguang ^a,b   Li, Xiaoying ^a,b   Ning, Guang ^a,b  

^a SHANGHAI JIAO TONG UNIVERSITY SCHOOL OF MEDICINE   (China)

^b Shanghai Institute of Immunology   (China)

Author keywords

Epithelial sodium channel; Hereditary disease; Hypertension; Liddle's syndrome

Indexed keywords

PROLINE; PROTEIN SCNN1B; SODIUM CHANNEL; UBIQUITIN PROTEIN LIGASE NEDD4; UNCLASSIFIED DRUG;

ADULT; ARTICLE; BIOINFORMATICS; CARBOXY TERMINAL SEQUENCE; CLINICAL FEATURE; CONTROLLED STUDY; GENE FUNCTION; GENE IDENTIFICATION; GENE LOCATION; GENE MUTATION; GENE STRUCTURE; GENETIC ANALYSIS; GENETIC VARIABILITY; HUMAN; LABORATORY TEST; LIDDLE SYNDROME; MALE; MISSENSE MUTATION; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN INTERACTION; PROTEIN MOTIF;

EID: 33748492735     PISSN: 1355008X     EISSN: 15590100     Source Type: Journal    
DOI: 10.1385/ENDO:29:3:385     Document Type: Article

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