SMCHD1 variants induce variegated expression in Facio Scapulo Humeral Dystrophy and Bosma Arhinia and microphtalmia syndrome (Methylation).

ABSTRACT: Determination of SMCHD1 epi-signature in type 2 Facio Scapulo Humeral Dystrophy (FSHD2) and Bosma Arhinia and Microphtalmia Syndrome (BAMS).

ORGANISM(S): Homo sapiens

PROVIDER: GSE175527 | GEO | 2023/12/31

REPOSITORIES: GEO