Autosomal recessive limbgirdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ–sarcoglycan gene

Author:

Nigro Vincenzo,Moreira Eloisa de Sá,Piluso Giulio,Vainzof Mariz,Belsito Angela,Politano Luisa,Puca Annibale A.,Passos-Bueno Maria Rita,Zatz Mayana

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Reference24 articles.

1. Bushby, K.M.D. & Beckmann, J.S. The limb-girdle muscular dystrophies — proposal for a new nomenclature. Neuromusc, Disord. 5, 337–343 (1995).

2. Walton, J.N. & Gardner-Medwin, D. The muscular dystrophies. in Disorders of voluntary muscle. (5th edn. ed. John Walton, Churchill Livingstone, 1988).

3. Speer, M. et al. Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy:linkage of an autosomal dominant form to chromosome5q. Am. J. Hum. Genet. 50, 1211–1217 (1992).

4. Beckmann, J.S. et al. A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkage analysis. C.R. Acad. Sci. Paris t312, 141–148 (1991).

5. Bashir, R. et al. A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p. Hum.Mol. Genet. 3, 455–457 (1994).

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