Limb-girdle type muscular dystrophy in a large family with distal myopathy: homozygous manifestation of a dominant gene?-Reference-Cited by-同舟云学术

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Limb-girdle type muscular dystrophy in a large family with distal myopathy: homozygous manifestation of a dominant gene?

Published:1992-06-01 Issue:6 Volume:29 Page:383-389
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Udd B

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference24 articles.

1. Clinical concepts of Duchenne muscular dystrophy;Rowland, L.P.;Brain,1988

2. Location of fascioscapulohumeral muscular dystrophy gene on chromosome 4;Wijmenga, C.; Frants, R.R.; Brouwer, O.F.; Moerer, P.; Weber, J.L.; Padberg, G.W.;Lancet,1990

3. On the classification, natural history and treatment of the myopathies;Walton, J.N.; Nattrass, F.J.;Brain,1954

4. The limb girdle syndromes;Bradley, W.G.,1979

5. Limb-girdle syndromes;RW, Jr, Shields,1986

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