Physical and genetic characterization of the distal segment of the myotonic dystrophy area on 19q.

doi:10.1016/0888-7543(92)90118-c

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Article

Physical and genetic characterization of the distal segment of the myotonic dystrophy area on 19q.

Genomics - 1 Jul 1992

Jansen G, de Jong P J, Amemiya C, Aslanidis C, Shaw D J, Harley H G, Brook J D, Fenwick R, Korneluk R G, Tsilfidis C

Abstract excerpt

The mutation involved in myotonic dystrophy (DM) has been mapped to the region between the ERCC1 DNA repair gene and the anonymous D19S51 locus on 19q13.3. Starting at locus D19S112 (probe pX75b), which served as a novel entry site for this chromosome region, we have established a cosmid contig o...

Topics

Base Sequence
Chromosome Mapping
Chromosomes, Human, Pair 19
Cloning, Molecular
Cosmids
DNA
DNA Probes
Female
Genetic Linkage
Genetic Markers
Humans
Male
Molecular Sequence Data
Mutation
Myotonic Dystrophy
Pedigree
Repetitive Sequences, Nucleic Acid

Source

Open in PubMed

Identifiers

PMID: 1639379
DOI: 10.1016/0888-7543(92)90118-c

Genes

ERCC1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-1639379-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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