A missense mutation in the αB-crystallin chaperone gene causes a desmin-related myopathy-Reference-Cited by-同舟云学术

A missense mutation in the αB-crystallin chaperone gene causes a desmin-related myopathy

Published:1998-09 Issue:1 Volume:20 Page:92-95
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Vicart Patrick,Caron Anne,Guicheney Pascale,Li Zhenlin,Prévost Marie-Christine,Faure Armelle,Chateau Danielle,Chapon Françoise,Tomé Fernando,Dupret Jean-Marie,Paulin Denise,Fardeau Michel

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0998_92.pdf

Reference30 articles.

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2. Fuchs, E. & Cleveland, D. A structural scaffolding of intermediate filaments in health and disease. Science 279, 514–519 (1998).

3. Bhat, S. & Nagineni, C. αB subunit of lens-specific protein α-crystallin is present in other ocular and nonocular tissue. Biochem. Biophys. Res. Commun. 158, 319–325 (1989).

4. Dubin, R., Wawrousek, E. & Piatigorsky, J. Expression of the murine αB-crystallin is not restricted to the lens. Mol. Cell Biol. 9, 1083–1091 (1989).

5. Graw, J. The crystallins: genes, proteins and diseases. Biol. Chem. 378, 1331–1348 (1997).

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