Sign Up to like & get
recommendations!
1
Published in 2020 at "Genes"
DOI: 10.3390/genes11030258
Abstract: 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…
read more here.
Keywords:
methylation;
fshd;
d4z4;
dna methylation ... See more keywords