Design, set-up and utility of the UK facioscapulohumeral muscular dystrophy patient registry-Reference-Cited by-同舟云学术

Design, set-up and utility of the UK facioscapulohumeral muscular dystrophy patient registry

Published:2016-05-09 Issue:7 Volume:263 Page:1401-1408
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

Evangelista Teresinha,Wood Libby,Fernandez-Torron Roberto,Williams Maggie,Smith Debbie,Lunt Peter,Hudson Judith,Norwood Fiona,Orrell Richard,Willis Tracey,Hilton-Jones David,Rafferty Karen,Guglieri Michela,Lochmüller Hanns

Funder

Muscular Dystrophy UK

Medical Research Council

Seventh Framework Programme

Publisher

Springer Science and Business Media LLC

Subject

Clinical Neurology,Neurology

Link

http://link.springer.com/content/pdf/10.1007/s00415-016-8132-1.pdf

Reference24 articles.

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2. Flanigan KM et al (2001) Genetic characterization of a large, historically significant Utah kindred with facioscapulohumeral dystrophy. Neuromuscul Disord 11(6–7):525–529

3. Mostacciuolo ML et al (2009) Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample. Clin Genet 75(6):550–555

4. Richards M et al (2012) Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled? Hum Genet 131(3):325–340

5. Hewitt JE et al (1994) Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy. Hum Mol Genet 3(8):1287–1295

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