Transcriptomics

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SMCHD1 variants induce variegated expression in Facio Scapulo Humeral Dystophy and Bosma Arhinia and microphtalmia syndrome. [RNA-Seq]

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: GSE174604 | GEO | 2022/05/27

REPOSITORIES: GEO

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