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

Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

1 Jun 1995

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 Genetic Neurodegenerative Diseases
Share to Laser Applications in Dentistry and Medicine
Share to Muscle Physiology and Disorders

Source

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 7663524
DOI: 10.1038/ng0695-243

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severityPMID 7663524Read ↗

Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophy.Semantic proximity Read ↗

Primary adhalin deficiency as a cause of muscular dystrophy in patients with normal dystrophin.Semantic proximity Read ↗

From adhalinopathies to alpha-sarcoglycanopathies: an overview.Semantic proximity Read ↗

Adhalin gene mutations in patients with autosomal recessive childhood onset muscular dystrophy with adhalin deficiency.Semantic proximity Read ↗

Neuromuscular Disorders: Clinical and Molecular GeneticsSemantic proximity Read ↗

[Early onset adhalinopathy (LGMD2D) mimicking congenital muscular dystrophy].Semantic proximity Read ↗

[Clinicopathological characteristics and molecular genetics of adhalin deficiency (severe childhood autosomal recessive muscular dystrophy/SCARMD)].Semantic proximity Read ↗

Bi-allelic ADPRHL2 Mutations Cause Neurodegeneration with Developmental Delay, Ataxia, and Axonal NeuropathySemantic proximity Read ↗

The Emery-Dreifuss Muscular Dystrophy Mutation Database.Semantic proximity Read ↗

Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian populationSemantic proximity Read ↗

Expanding the phenotype associated with missense mutations of the ARX gene.Semantic proximity Read ↗

Hereditary AtaxiasSemantic proximity Read ↗

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