Clinical and histopathological heterogeneity in patients with 4q35 facioscapulohumeral muscular dystrophy (FSHD)
Author:
Publisher
Wiley
Subject
Physiology (medical),Neurology (clinical),Neurology,Histology,Pathology and Forensic Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.0305-1846.2003.00520.x/fullpdf
Reference11 articles.
1. Location of facioscapulohumeral muscular dystrophy on chromosome 4;Wijmenga;Lancet,1990
2. FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2kb tandemly repeated unit;Van Deutekom;Hum Mol Genet,1993
3. Inappropriate gene activation in FSHD. A repressor complex binds a chromosomal repeat deleted in dystrophic muscle;Gabellini;Cell,2002
4. Definitive molecular diagnosis of facioscapulohumeral dystrophy;Orrell;Neurology,1999
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