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Does DNA Methylation Matter in FSHD?
Facioscapulohumeral muscular dystrophy (FSHD) has been associated with the genetic and epigenetic molecular features of the CpG-rich D4Z4 repeat tandem array at 4q35. Reduced DNA methylation of D4Z4 repeats is considered part of the FSHD mechanism and has been proposed as a reliable marker in the FS...
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| Published in: | Genes (Basel) |
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| Main Authors: | , , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
MDPI
2020
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| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7140823/ https://ncbi.nlm.nih.gov/pubmed/32121044 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes11030258 |
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