Liddle's syndrome caused by a novel mutation of the γ-subunit of epithelial sodium channel gene SCNN1G in Chinese

Chinese Journal of Medical Genetics

Volumn 27, Issue 2, 2010, Pages 132-135

  Shi, Jin Yu ^a   Chen, Xiang ^a   Ren, Yan ^a   Long, Yang ^a   Tian, Hao Ming ^a  

^a SICHUAN UNIVERSITY   (China)

Author keywords

Epithelial sodium channel; Gene mutation; Liddle's syndrome

Indexed keywords

ALDOSTERONE; EPITHELIAL SODIUM CHANNEL; GENOMIC DNA; PROTEIN SCNN1B; PROTEIN SCNN1G; UNCLASSIFIED DRUG;

ALDOSTERONE BLOOD LEVEL; ARTICLE; BLOOD; CHINESE; CODON; DNA SEQUENCE; EXON; GENE AMPLIFICATION; HETEROZYGOTE; HUMAN; LIDDLE SYNDROME; NONSENSE MUTATION; PLASMA RENIN ACTIVITY; POLYMERASE CHAIN REACTION; SCREENING TEST;

ADULT; ASIAN CONTINENTAL ANCESTRY GROUP; BASE SEQUENCE; CASE-CONTROL STUDIES; DNA MUTATIONAL ANALYSIS; EPITHELIAL SODIUM CHANNEL; FEMALE; HUMANS; LIDDLE SYNDROME; MALE; MUTATION; PEDIGREE; YOUNG ADULT;

EID: 77951979478     PISSN: 10039406     EISSN: None     Source Type: Journal    
DOI: 10.3760/cma.j.issn.1003-9406.2010.02.003     Document Type: Article

References (7)

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