Art

J-GLOBAL ID：200902148736327510   Reference number：01A0725734

Molecular Etiology of Idiopathic Cardiomyopathy in Asian Populations.

アジア人集団における特発性心筋症の分子病因学

Author (5)： KIMURA A (Tokyo Medical and Dental Univ., Tokyo, JPN) ,  ITO-SATOH M (Tokyo Medical and Dental Univ., Tokyo, JPN) ,  HAYASHI T (Tokyo Medical and Dental Univ., Tokyo, JPN) ,  TAKAHASHI M (Tokyo Medical and Dental Univ., Tokyo, JPN) ,  ARIMURA T (Tokyo Medical and Dental Univ., Tokyo, JPN)
Material： Journal of Cardiology  (J Cardiol)
Volume： 37  Issue： Supplement 1  Page： 139-146  Publication year： Jun. 15, 2001 
JST Material Number： Y0264A  ISSN： 0914-5087  Document type： Article
Country of issue： Japan (JPN)  Language： ENGLISH (EN)

Reference (48)：

• GEISTERFER-LOWRANCE, AA. A molecular basis for familial hypertrophic cardiomyopathy : A beta cardiac myosin heavy chain gene missense mutation. Cell. 1990, 62, 999-1006
• JARCHO, JA. Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1. N Engl J Med. 1989, 321, 1372-1378
• WATKINS, H. A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3. Nat Genet. 1993, 3, 333-337
• THIERFELDER, L. Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy : A disease of the sarcomere. Cell. 1994, 77, 701-712
• THIERFELDER, L. A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2. Proc Natl Acad Sci USA. 1993, 90, 6270-6274

Terms in the title (5)： アジア人 ,  集団 ,  特発性心筋症 ,  分子 ,  病因学