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Direct interplay between two candidate genes in FSHD muscular dystrophy
Facioscapulohumeral muscular dystrophy (FSHD) is one of the most common neuromuscular disorders. The major form of the disease (FSHD1) is linked to decrease in copy number of a 3.3-kb tandem repeated macrosatellite (D4Z4), located on chromosome 4q35. D4Z4 deletion alters chromatin structure of the l...
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| Udgivet i: | Hum Mol Genet |
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| Main Authors: | , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Oxford University Press
2015
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4321439/ https://ncbi.nlm.nih.gov/pubmed/25326393 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddu536 |
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