Normal growth and regenerating ability of myoblasts from unaffected muscles of facioscapulohumeral muscular dystrophy patients-Reference-Cited by-同舟云学术

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Normal growth and regenerating ability of myoblasts from unaffected muscles of facioscapulohumeral muscular dystrophy patients

Published:2005-06-16 Issue:22 Volume:12 Page:1651-1662
ISSN:0969-7128
Container-title:Gene Therapy
language:en
Short-container-title:Gene Ther

Author:

Vilquin J-T,Marolleau J-P,Sacconi S,Garcin I,Lacassagne M-N,Robert I,Ternaux B,Bouazza B,Larghero J,Desnuelle C

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Molecular Medicine

Link

http://www.nature.com/articles/3302565.pdf

Reference58 articles.

1. Lunt P . Facioscapulohumeral muscular dystrophy: diagnostic and molecular aspects. In: Deymeer F (ed). Neuromuscular Diseases: From Basic Mechanisms to Clinical Management. Monographs in Clinical Neuroscience, Vol. 18. Karger: Basel, Freiburg, Paris, London, New York, New Delhi, Bangkok, Singapore, Tokyo, Sydney, 2000: 44–60.

2. Wijmenga C et al. Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy. Nat Genet 1992; 2: 26–33.

3. Hewitt JE et al. Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy. Hum Mol Genet 1994; 3: 1287–1295.

4. Lunt PW et al. Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD). Hum Mol Genet 1995; 4: 951–958.

5. Tawil R et al. Evidence for anticipation and association of deletion size with severity in facioscapulohumeral muscular dystrophy. Ann Neurol 1996; 39: 744–748.

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