[Role of associated alleles and hypomethylation status in the clinical expression of facioscapulohumeral muscular dystrophy].

Pikó, Henriett

[Role of associated alleles and hypomethylation status in the clinical expression of facioscapulohumeral muscular dystrophy]. [electronic resource] - Orvosi hetilap Sep 2011 - 1576-85 p. digital

Publication Type: English Abstract; Journal Article

0030-6002

10.1556/OH.2011.29179 doi


Alleles
Blotting, Southern
Chromosomes, Human, Pair 4--genetics
DNA Methylation
Epigenesis, Genetic
Humans
Muscular Dystrophy, Facioscapulohumeral--genetics
Phenotype
Repetitive Sequences, Nucleic Acid
Telomere--genetics