Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy-Reference-Cited by-同舟云学术

Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy

Published:2002-07 Issue:6896 Volume:418 Page:422-425
ISSN:0028-0836
Container-title:Nature
language:en
Short-container-title:Nature

Author:

Moore Steven A.,Saito Fumiaki,Chen Jianguo,Michele Daniel E.,Henry Michael D.,Messing Albee,Cohn Ronald D.,Ross-Barta Susan E.,Westra Steve,Williamson Roger A.,Hoshi Toshinori,Campbell Kevin P.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/nature00838.pdf

Reference30 articles.

1. Fukuyama, Y., Osawa, M. & Suzuki, H. Congenital progressive muscular dystrophy of the Fukuyama type—clinical, genetic and pathological considerations. Brain Dev. 3, 1–29 (1981)

2. Kobayashi, K. et al. An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy. Nature 394, 388–392 (1998)

3. Cormand, B. et al. Clinical and genetic distinction between Walker–Warburg syndrome and muscle-eye-brain disease. Neurology 56, 1059–1069 (2001)

4. Haltia, M. et al. Muscle-eye-brain disease: a neuropathological study. Ann. Neurol. 41, 173–180 (1997)

5. Yoshida, A. et al. Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1. Dev. Cell 1, 717–724 (2001)

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