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Article

Long-range restriction map around the Duchenne muscular dystrophy gene.

Nature - 1 Jan 2000

Burmeister M, Lehrach H

Abstract excerpt

Duchenne muscular dystrophy is an X-linked recessive disease affecting about 1 in 4,000 newborn boys. As in many other inherited diseases, the biochemical basis of the condition is unknown, and as yet there is no effective treatment. Translocations, deletions and other mutations leading to the DMD phenotype are distributed over a chromosomal area of large, but unknown size. Using pulsed-field gradient gel...

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Source

Identifiers

PMID: 3024018
DOI: 10.1038/324582a0

Genes

DMD

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

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Long-range restriction map around the Duchenne muscular dystrophy gene.PMID 3024018Read ↗

Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment.Semantic proximity Read ↗

Duplicational mutation at the Duchenne muscular dystrophy locus: its frequency, distribution, origin, and phenotypegenotype correlation.Semantic proximity Read ↗

Direct detection of more than 50% of the Duchenne muscular dystrophy mutations by field inversion gels.Semantic proximity Read ↗

Transcriptional and epigenetic analyses of the DMD locus reveal novel cis‑acting DNA elements that govern muscle dystrophin expression.Semantic proximity Read ↗

Molecular analysis of human muscular dystrophies.Semantic proximity Read ↗

Deletions, duplications and novel restriction fragment length polymorphism in Duchenne and Becker muscular dystrophies.Semantic proximity Read ↗

Analysis of RFLPs and DNA deletions in the Chinese Duchenne muscular dystrophy gene.Semantic proximity Read ↗

Precise mapping of 17 deletion breakpoints within the central hotspot deletion region (introns 50 and 51) of the DMD gene.Semantic proximity Read ↗

Exonic rearrangements in DMD in Chinese Han individuals affected with Duchenne and Becker muscular dystrophies.Semantic proximity Read ↗

YAC/STS map of 15Mb of Xp21.3-p11.3, at 100kb resolution, with refined comparisons of genetic distances and DMD structure.Semantic proximity Read ↗

Molecular deletion patterns in families from southern France with Duchenne/Becker muscular dystrophies.Semantic proximity Read ↗

Isolation, physical mapping, and Northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2Semantic proximity Read ↗

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