Myoblasts from affected and non-affected FSHD muscles exhibit morphological differentiation defects
Author:
Publisher
Wiley
Subject
Cell Biology,Molecular Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1582-4934.2008.00368.x/fullpdf
Reference39 articles.
1. FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit;Van Deutekom;Hum Mol Genet,1993
2. Characterization of a tandemly repeated 3.3-kb KpnI unit in the facioscapulohumeral muscular dystrophy (FSHD) gene region on chromosome 4q35;Lee;Muscle Nerve,1995
3. Phenotypic-genotypic correlation will assist genetic counseling in 4q35-facioscapulohumeral muscular dystrophy;Lunt;Muscle Nerve,1995
4. Pulsed-field gel electrophoresis of the D4F104S1 locus reveals the size and the parental origin of the facioscapulohumeral muscular dystrophy (FSHD)-associated deletions;Wijmenga;Genomics,1994
5. 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);Lunt;Hum Mol Genet,1995
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