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Dystrophin-associated proteins in muscular dystrophy

Ozawa, E, Yoshida, M, Suzuki, A, Mizuno, Y, Hagiwara, Y, Noguchi, S·1995·Human Molecular Genetics

Abstract

Dystrophin-associated proteins (DAPs) are classified into a few groups, namely, those comprising of dystroglycan complex, sarcoglycan complex, syntrophin complex and others. Subsarcolemmal actin filaments are connected to laminin in the basement membrane through dystrophin and the dystroglycan complex. This system may function to protect muscle fibers from mechanical damage. Furthermore, the sarcoglycan complex is associated with the system. Defects in the components of the protection system or the sarcoglycan complex or both are characteristically found in various muscular dystrophies. The roles of the syntrophin complex are meagerly understood. In this review, the possible roles of laminin, DAPs and dystrophin in each dystrophy are explained.

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Metadata

Authors
Ozawa, E., Yoshida, M., Suzuki, A., Mizuno, Y., Hagiwara, Y., & Noguchi, S.
Venue
Human Molecular Genetics
Published
1995-09-01
Volume
4
Issue
suppl_1
Pages
1711-1716
ISSN
  • 0964-6906 (ISSN-L)
  • 1460-2083
OpenAlex
W1525849227
Cited by
242
References
0
FWCI
10.18
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Dystrophin-associated proteins in muscular dystrophy. https://app.cochat.ai/papers/10.1093/hmg/4.suppl_1.1711
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Ozawa, E., Yoshida, M., Suzuki, A., Mizuno, Y., Hagiwara, Y., & Noguchi, S. (1995). Dystrophin-associated proteins in muscular dystrophy. Human Molecular Genetics. https://doi.org/10.1093/hmg/4.suppl_1.1711

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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