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Mapping of a chromosome 15 region involved in limb girdle muscular dystrophy.

Human molecular genetics - 1 Feb 1994

Fougerousse F, Broux O, Richard I, Allamand V, de Souza A P, Bourg N, Brenguier L, Devaud C, Pasturaud P, Roudaut C

Abstract excerpt

A gene responsible for an autosomal recessive form of limb girdle muscular dystrophy (LGMD2, MIM number 253600) has been localized on chromosome 15. After genotyping additional markers of this chromosome, two were found to flank the disease locus within an interval that was assessed as 7 centiMorgans. The screening of the CEPH YAC libraries with the corresponding probes allowed the isolation of YACs which were...

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Source

Identifiers

PMID: 8004096
DOI: 10.1093/hmg/3.2.285

Genes

STS

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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.

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Mapping of a chromosome 15 region involved in limb girdle muscular dystrophy.PMID 8004096Read ↗

Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15q15.1-q15.3 interval.Semantic proximity Read ↗

A primary expression map of the chromosome 15q15 region containing the recessive form of limb-girdle muscular dystrophy (LGMD2A) geneSemantic proximity Read ↗

Limb-girdle muscular dystrophy is closely linked to the fibrillin locus on chromosome 15.Semantic proximity Read ↗

Regional localization of human chromosome 15 loci.Semantic proximity Read ↗

Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in Brazilian families.Semantic proximity Read ↗

A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p.Semantic proximity Read ↗

A linkage map of human chromosome 15 with an average resolution of 2 cM and containing 55 polymorphic microsatellites.Semantic proximity Read ↗

The CEPH consortium linkage map of human chromosome 15q.Semantic proximity Read ↗

Use of a CEPH meiotic breakpoint panel to refine the locus of limb-girdle muscular dystrophy type 1A (LGMD1A) to a 2-Mb interval on 5q31.Semantic proximity Read ↗

Sequence analysis of 21 genes located in the Kartagener syndrome linkage region on chromosome 15qSemantic proximity Read ↗

Genetic and Physical Mapping of the Locus for Autosomal Dominant Renal Fanconi Syndrome, on Chromosome 15q15.3Semantic proximity Read ↗

Mouse chromosome 15.Semantic proximity Read ↗

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