Genetic analysis in patients with left ventricular noncompaction and evidence for genetic heterogeneity-Reference-Cited by-同舟云学术

Genetic analysis in patients with left ventricular noncompaction and evidence for genetic heterogeneity

Published:2006-05 Issue:1 Volume:88 Page:71-77
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Xing Yanlin,Ichida Fukiko,Matsuoka Taro,Isobe Takeshi,Ikemoto Yumiko,Higaki Takashi,Tsuji Tohru,Haneda Noriyuki,Kuwabara Atsushi,Chen Rui,Futatani Takeshi,Tsubata Shinichi,Watanabe Sayaka,Watanabe Kazuhiro,Hirono Keiichi,Uese Keiichiro,Miyawaki Toshio,Bowles Karla R.,Bowles Neil E.,Towbin Jeffrey A.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference28 articles.

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2. Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the definition and classification of cardiomyopathies;Richardson;Circulation,1996

3. Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome;Ichida;Circulation,2001

4. Mutation analysis of the G4.5 gene in patients with isolated left ventricular noncompaction;Chen;Mol. Genet. Metab.,2002

5. Isolated left ventricular noncompaction is rarely caused by mutations in G4.5, α-dystrobrevin and FK Binding Protein-12;Kenton;Mol. Genet. Metab.,2004

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