Cis D4Z4 repeat duplications associated with facioscapulohumeral muscular dystrophy type 2

Facioscapulohumeral muscular dystrophy, known in genetic forms FSHD1 and FSHD2, is associated with D4Z4 repeat array chromatin relaxation and somatic derepression of DUX4 located in D4Z4. A complete copy of DUX4 is present on 4qA chromosomes, but not on the D4Z4-like repeats of chromosomes 4qB or 10...

Full description

Saved in:
Bibliographic Details
Published in:Hum Mol Genet
Main Authors: Lemmers, Richard J L F, van der Vliet, Patrick J, Vreijling, Jeroen P, Henderson, Don, van der Stoep, Nienke, Voermans, Nicol, van Engelen, Baziel, Baas, Frank, Sacconi, Sabrina, Tawil, Rabi, van der Maarel, Silvère M
Format: Artigo
Language:Inglês
Published: Oxford University Press 2018
Subjects:
General Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC6168970/
https://ncbi.nlm.nih.gov/pubmed/30281091
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddy236
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items