Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)-Reference-Cited by-同舟云学术

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

Published:2000-08 Issue:6798 Volume:406 Page:906-910
ISSN:0028-0836
Container-title:Nature
language:en
Short-container-title:Nature

Author:

Nishino Ichizo,Fu Jin,Tanji Kurenai,Yamada Takeshi,Shimojo Sadatomo,Koori Tateo,Mora Marina,Riggs Jack E.,Oh Shin J.,Koga Yasutoshi,Sue Carolyn M.,Yamamoto Ayaka,Murakami Nobuyuki,Shanske Sara,Byrne Edward,Bonilla Eduardo,Nonaka Ikuya,DiMauro Salvatore,Hirano Michio

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/35022604.pdf

Reference29 articles.

1. Danon, M. J. et al. Lysosomal glycogen storage disease with normal acid maltase. Neurology 31, 51–57 (1981).

2. Muntoni, F. et al. Familial cardiomyopathy, mental retardation and myopathy associated with desmin-type intermediate filaments. Neuromusc. Disord. 4, 233–241 (1994).

3. Murakami, N. et al. Sarcolemmal indentation in cardiomyopathy with mental retardation and vacuolar myopathy. Neuromusc. Disord. 5, 149–155 (1995).

4. Tanaka, Y. et al. Accumulation of autophagic vacuoles and cardiomyopathy in LAMP-2 deficient mice. Nature 406, 902– 906 (2000).

5. Fukuda, M. Biogenesis of the lysosomal membrane. Subcell. Biochem. 22, 199–230 (1994).

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