Chromatin loop domain organization within the 4q35 locus in facioscapulohumeral dystrophy patients versus normal human myoblasts

Fascioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant neuromuscular disorder linked to partial deletion of integral numbers of a 3.3 kb polymorphic repeat, D4Z4, within the subtelomeric region of chromosome 4q. Although the relationship between deletions of D4Z4 and FSHD is well es...

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Bibliographic Details
Main Authors: Petrov, Andrei, Pirozhkova, Iryna, Carnac, Gilles, Laoudj, Dalila, Lipinski, Marc, Vassetzky, Yegor S.
Format: Artigo
Language:Inglês
Published: National Academy of Sciences 2006
Subjects:
Biological Sciences
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC1459005/
https://ncbi.nlm.nih.gov/pubmed/16632607
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0511235103
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