Art

J-GLOBAL ID：200902194519548861   Reference number：01A0982493

Genetic Alterations in Patients with Primary Aldosteronism.

原発性アルドステロン症患者における遺伝学的変化

Author (1)： TAKEDA Y (Kanazawa Univ., Kanazawa, JPN)
Material： Hypertension Research  (Hypertens Res)
Volume： 24  Issue： 5  Page： 469-474  Publication year： Sep. 2001 
JST Material Number： Y0303A  ISSN： 0916-9636  Document type： Article
Article type： 解説  Country of issue： Germany, Federal Republic of (DEU)  Language： ENGLISH (EN)

Thesaurus term： *hyperaldosteronism ,...
Semi thesaurus term： primary aldosteronism ,...

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JST classification (2)： Endocrine diseases  (GL03000I) ,  Genetic variation  (EC01030Y)

Reference (50)：

• 1. Hansson JH, Nelson-Williams C, Suzuki H, et al: Hypertension caused by a truncated epithelial sodium channel gamma subunit: genetic heterogeneity of Liddle syndrome. Nat Genet 1995; 11: 76-82.
• 2. Wilson RC, Harbison MD, Krozowski ZS, et al: Several homozygous mutations in the gene for 11β-hydroxysteroid dehydrogenase type 2 in patients with apparent mineralocorticoid excess. J Clin Endocrinol Metab 1995; 80: 3145-3150.
• 3. Mune T, Rogerson FM, Nillila H, et al: Human hypertension caused by mutations in the kidney isozyme of 11β-hydroxysteroid dehydrogenase. Nat Genet 1995; 10: 394-399.
• 4. Geller DS, Farhi A, Pinkerton N, et al: Activating mineralocorticoid receptor mutations in hypertension exacerbated by pregnancy. Science 2000; 289: 119-122.
• 5. Lafferty AR, Torpy DJ, Stowasser M, et al: A novel genetic locus for low renin hypertension: familial hyperaldosteronism type II maps to chromosome 7 (7p22). J Med Genet 2000; 37: 831-835.

Terms in the title (3)： 原発性アルドステロン症 ,  患者 ,  遺伝学