Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

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

11 Aug 2015

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Congenital heart defects research
Share to Muscle Physiology and Disorders
Share to Tissue Engineering and Regenerative Medicine

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 26319123
DOI: 10.1016/j.nmd.2015.08.004

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Low D4Z4 copy number and gender difference in Korean patients with facioscapulohumeral muscular dystrophy type 1PMID 26319123Read ↗

The D4Z4 repeat-mediated pathogenesis of facioscapulohumeral muscular dystrophy.Semantic proximity Read ↗

Molecular genetics of facioscapulohumeral muscular dystrophy (FSHD)Semantic proximity Read ↗

Phenotypic Variability Among Patients With D4Z4 Reduced Allele Facioscapulohumeral Muscular Dystrophy.Semantic proximity Read ↗

Large genotype-phenotype study in carriers of D4Z4 borderline alleles provides guidance for facioscapulohumeral muscular dystrophy diagnosis.Semantic proximity Read ↗

The Role of Whole-Exome Sequencing and Methylation Analysis in Untangling Complex Facioscapulo-Humeral Muscular Dystrophy Cases.Semantic proximity Read ↗

Telomere position effect regulates DUX4 in human facioscapulohumeral muscular dystrophySemantic proximity Read ↗

Introduction: the expansion of clinical and molecular genetic knowledge in facioscapulohumeral muscular dystrophy (FSHD).Semantic proximity Read ↗

Pearls in the junk: dissecting the molecular pathogenesis of facioscapulohumeral muscular dystrophy.Semantic proximity Read ↗

The China facioscapulohumeral muscular dystrophy type 1 (FSHD1) registry: rationale for and description of a nationwide, observational cohort studySemantic proximity Read ↗

Case Studies on the Genetic and Clinical Diagnosis of Facioscapulohumeral Muscular Dystrophy.Semantic proximity Read ↗

[Clinical phenotype and genotype of early-onset facioscapulohumeral muscular dystrophy type 1].Semantic proximity Read ↗

Genetic modifiers of <scp>D</scp>uchenne and facioscapulohumeral muscular dystrophiesSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.