Genotype, phenotype, and follow-up in Taiwanese patients with salt-losing tubulopathy associated with SLC12A3 mutation

Journal of Clinical Endocrinology and Metabolism

Volumn 97, Issue 8, 2012, Pages

  Tseng, Min Hua ^a,c   Yang, Sung Sen ^b,c   Hsu, Yu Juei ^b,c   Fang, Yu Wei ^c,d   Wu, Chih Jen ^e   Tsai, Jeng Daw ^e   Hwang, Daw Yang ^f   Lin, Shih Hua ^b,c  

^a CHANG GUNG MEMORIAL HOSPITAL   (Taiwan)

^b TRI SERVICE GENERAL HOSPITAL   (Taiwan)

^c NATIONAL DEFENSE MEDICAL CENTER   (Taiwan)

^d SHIN KONG WU HO SU MEMORIAL HOSPITAL   (Taiwan)

^e TAIPEI MEDICAL UNIVERSITY   (Taiwan)

^f KAOHSIUNG MEDICAL UNIVERSITY   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

ALDOSTERONE; SODIUM CHLORIDE COTRANSPORTER;

ADULT; ALDOSTERONE BLOOD LEVEL; ARTICLE; CHRONIC KIDNEY DISEASE; FEMALE; FOLLOW UP; GENE; GENE MUTATION; GENETIC ASSOCIATION; GENOTYPE; GITELMAN SYNDROME; HOMOZYGOSITY; HUMAN; HYPOCALCIURIA; HYPOKALEMIA; HYPOMAGNESEMIA; INTRON; MAJOR CLINICAL STUDY; MALE; NON INSULIN DEPENDENT DIABETES MELLITUS; ONSET AGE; PHENOTYPE; PRIORITY JOURNAL; SEX DIFFERENCE; SLC12A3 GENE; TAIWAN;

ADOLESCENT; ADULT; AGE OF ONSET; FEMALE; FOLLOW-UP STUDIES; GENOTYPE; GITELMAN SYNDROME; HUMANS; MALE; MUTATION; PHENOTYPE; RECEPTORS, DRUG; SYMPORTERS; TAIWAN;

EID: 84864823801     PISSN: 0021972X     EISSN: 19457197     Source Type: Journal    
DOI: 10.1210/jc.2012-1707     Document Type: Article

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