Low D4Z4 copy number and gender difference in Korean patients with facioscapulohumeral muscular dystrophy type 1-Reference-Cited by-同舟云学术

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Low D4Z4 copy number and gender difference in Korean patients with facioscapulohumeral muscular dystrophy type 1

Published:2015-11 Issue:11 Volume:25 Page:859-864
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Park Hyung Jun,Hong Ji-Man,Lee Jung Hwan,Lee Hyung Seok,Shin Ha Young,Kim Seung Min,Ki Chang-Seok,Lee Ji Hyun,Choi Young-Chul

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference26 articles.

1. Population-based incidence and prevalence of facioscapulohumeral dystrophy;Deenen;Neurology,2014

2. Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy;Wijmenga;Nat Genet,1992

3. Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy;van Overveld;Nat Genet,2003

4. Specific loss of histone H3 lysine 9 trimethylation and HP1gamma/cohesin binding at D4Z4 repeats is associated with facioscapulohumeral dystrophy (FSHD);Zeng;PLoS Genet,2009

5. Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled?;Richards;Hum Genet,2012

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1. A novel family of lncRNAs relate facioscapulohumeral muscular dystrophy to nucleolar architecture and protein synthesis;2024-06-29

2. Clinical Application of Optical Genome Mapping for Molecular Diagnosis of Facioscapulohumeral Muscular Dystrophy;Annals of Laboratory Medicine;2024-05-10

3. Best practice guidelines on genetic diagnostics of facioscapulohumeral muscular dystrophy: Update of the 2012 guidelines;Clinical Genetics;2024-04-29

4. The first genetically confirmed cohort of Facioscapulohumeral Muscular Dystrophy from Northern India;European Journal of Human Genetics;2024-04-25

5. ZNF142mutation causes sex-dependent neurologic disorder;Journal of Medical Genetics;2024-01-31

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