Novel LAMP-2 Mutation in a Family With Danon Disease Presenting With Hypertrophic Cardiomyopathy-Reference-Cited by-同舟云学术

Novel LAMP-2 Mutation in a Family With Danon Disease Presenting With Hypertrophic Cardiomyopathy

Published:2009 Issue:2 Volume:73 Page:376-380
ISSN:1346-9843
Container-title:Circulation Journal
language:en
Short-container-title:Circ J

Author:

Dougu Nobuhiro¹,Joho Shuji²,Shan Lishen³,Shida Takuya²,Matsuki Akira²,Uese Keiichiro³,Hirono Keiichi³,Ichida Fukiko³,Tanaka Kortaro¹,Nishino Ichizo⁴,Inoue Hiroshi²

Affiliation:

1. Department of Neurology, Toyama University Hospital

2. Second Department of Internal Medicine, Toyama University Hospital

3. Department of Pediatrics, Toyama University Hospital

4. Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry

Publisher

Japanese Circulation Society

Subject

Cardiology and Cardiovascular Medicine,General Medicine

Link

http://www.jstage.jst.go.jp/article/circj/73/2/73_CJ-08-0241/_pdf

Reference17 articles.

1. Hypertrophic Cardiomyopathy

2. Glycogen Storage Diseases Presenting as Hypertrophic Cardiomyopathy

3. Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)

4. 4. Sugie K, Yamamoto A, Murayama K, Oh SJ, Takahashi M, Mora M, et al. Clinicopathological features of genetically confirmed Danon disease. Neurology 2002; 58: 1773-1778.

5. Danon Disease as an Underrecognized Cause of Hypertrophic Cardiomyopathy in Children

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