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

Epilepsy and mental retardation in a subset of early onset 4q35-facioscapulohumeral muscular dystrophy.

Neurology - 1 Jun 1998

Funakoshi M, Goto K, Arahata K

Abstract excerpt

The gene for facioscapulohumeral muscular dystrophy (FSHD) has been mapped to chromosome 4q35. In most patients with FSHD, a deletion of 3.3 kb tandemly repeated units within the EcoRI fragment that can be detected by probe p13E-11 is associated with the disease. To elucidate the relation between...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Age of Onset
Share to Child

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Child, Preschool

Share to Gene Deletion

Share to Genotype

Share to Phenotype

Share to Repetitive Sequences, Nucleic Acid

Source

Identifiers

PMID: 9633729
DOI: 10.1212/wnl.50.6.1791

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Prepared record publication-9633729-2026-09-05.1. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Epilepsy and mental retardation in a subset of early onset 4q35-facioscapulohumeral muscular dystrophy.PMID 9633729Read ↗

[Clinical and genetical features of Japanese early-onset facioscapulohumeral muscular dystrophy].Semantic proximity Read ↗

[Facioscapulohumeral muscular dystrophy (FSHD)].Semantic proximity Read ↗

Typical facioscapulohumeral dystrophy phenotype in patients without FSHD 4q35 deletion.Semantic proximity Read ↗

Facioscapulohumeral muscular dystrophy: hearing loss and other atypical features of patients with large 4q35 deletions.Semantic proximity Read ↗

New Insights into Genotype-phenotype Correlations in Chinese Facioscapulohumeral Muscular Dystrophy: A Retrospective Analysis of 178 Patients.Semantic proximity Read ↗

[Genetic analysis of facioscapulohumeral muscular dystrophy (FSHD)].Semantic proximity Read ↗

Atypical phenotypes in patients with facioscapulohumeral muscular dystrophy 4q35 deletion.Semantic proximity Read ↗

The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than females.Semantic proximity Read ↗

Facioscapulohumeral muscular dystrophy: clinical diversity and genetic abnormalities in Japanese patients.Semantic proximity Read ↗

Evidence for subtelomeric exchange of 3.3 kb tandemly repeated units between chromosomes 4q35 and 10q26: implications for genetic counselling and etiology of FSHD1Semantic proximity Read ↗

Clinical and genetic analysis of Korean patients with facioscapulohumeral muscular dystrophy.Semantic proximity Read ↗

Facioscapulohumeral dystrophy.Semantic proximity Read ↗

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