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

Hereditary inclusion body myopathy maps to chromosome 9p1-q1.

Human molecular genetics - 1 Jan 1996

Mitrani-Rosenbaum S, Argov Z, Blumenfeld A, Seidman C E, Seidman J G

Abstract excerpt

Hereditary inclusion body myopathy (HIBM) is a unique disorder of unknown etiology that typically occurs in individuals of Persian Jewish descent. Distinguishing features of the disorder from other limb girdle myopathies include elderly age of onset, ethnic predisposition, and sparing of the quadriceps despite severe involvement of all other proximal leg muscles. Involved muscles demonstrate fibers with rimmed...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Mapping
Share to Chromosomes, Human, Pair 9
Share to Genotype

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Inclusion Bodies

Share to Lod Score

Share to Muscular Diseases

Share to Pedigree

Source

Identifiers

PMID: 8789455
DOI: 10.1093/hmg/5.1.159

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hereditary inclusion body myopathy maps to chromosome 9p1-q1.PMID 8789455Read ↗

Fine-structure mapping of the hereditary inclusion body myopathy locus.Semantic proximity Read ↗

Gene locus for autosomal recessive distal myopathy with rimmed vacuoles maps to chromosome 9.Semantic proximity Read ↗

The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy.Semantic proximity Read ↗

Hereditary inclusion body myopathy: the Middle Eastern genetic cluster.Semantic proximity Read ↗

The spectrum of familial inclusion body myopathies in 13 families and a description of a quadriceps-sparing phenotype in non-Iranian Jews.Semantic proximity Read ↗

Inclusion body myositis: from genetics to clinical trialsSemantic proximity Read ↗

Hereditary inclusion body myopathy in Persian Jews: a case report from Iran.Semantic proximity Read ↗

A novel autosomal recessive limb-girdle muscular dystrophy with quadriceps atrophy maps to 11p13-p12.Semantic proximity Read ↗

Genetics of inclusion-body myositis.Semantic proximity Read ↗

Clinical Delineation and Localization to Chromosome 9p13.3–p12 of a Unique Dominant Disorder in Four Families: Hereditary Inclusion Body Myopathy, Paget Disease of Bone, and Frontotemporal DementiaSemantic proximity Read ↗

New Developments in the Genetics of Inclusion Body Myositis.Semantic proximity Read ↗

Isolated inclusion body myopathy caused by a multisystem proteinopathy–linked <i>hnRNPA1</i> mutationSemantic proximity Read ↗

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