Differential DNA methylation of the D4Z4 repeat in patients with FSHD and asymptomatic carriers-Reference-Cited by-同舟云学术

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Differential DNA methylation of the D4Z4 repeat in patients with FSHD and asymptomatic carriers

Published:2014-07-16 Issue:8 Volume:83 Page:733-742
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Gaillard M.-C.,Roche S.,Dion C.,Tasmadjian A.,Bouget G.,Salort-Campana E.,Vovan C.,Chaix C.,Broucqsault N.,Morere J.,Puppo F.,Bartoli M.,Levy N.,Bernard R.,Attarian S.,Nguyen K.,Magdinier F.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 79 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Progesterone may be a regulator and B12 could be an indicator of the proximal D4Z4 repeat methylation status on 4q35ter;Journal of Neurochemistry;2024-08-06

2. Exchange of subtelomeric regions between chromosomes 4q and 10q reverts the FSHD genotype and phenotype;Science Advances;2024-05-03

3. SMCHD1 genetic variants in type 2 FacioScapuloHumeral dystrophy and challenges in predicting pathogenicity and disease penetrance.;2024-02-09

4. Case report: Identification of facioscapulohumeral muscular dystrophy 1 in two siblings with normal phenotypic parents using optical genome mapping;Frontiers in Neurology;2024-02-01

5. Deciphering D4Z4 CpG methylation gradients in fascioscapulohumeral muscular dystrophy using nanopore sequencing;Genome Research;2023-09

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