Genetic mapping near the myd locus on mouse chromosome 8.

doi:10.1007/BF00352416

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Article

Genetic mapping near the myd locus on mouse chromosome 8.

Mammalian genome : official journal of the International Mammalian Genome Society - 1 Apr 1995

Mills K A, Mathews K D, Scherpbier-Heddema T, Schelper R L, Schmalzel R, Bailey H L, Nadeau J H, Buetow K H, Murray J C

Abstract excerpt

Myodystrophy (myd), an autosomal recessive mutation of the mouse characterized by progressive weakness and dystrophic muscle histology, maps to the central portion of Chromosome (Chr) 8 (Lane et al. J. Hered 67, 135, 1976). This portion of Chr 8 contains the genes for a mitochondrial uncoupling protein (Ucp) and kallikrein (Kal3), which map to distal 4q in the human, providing evidence for a segment of homology....

Topics

Animals
Base Sequence
Chromosome Mapping
Chromosomes
Chromosomes, Human, Pair 4
Crosses, Genetic
Female
Genetic Linkage
Genetic Markers
Haplotypes
Humans

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Male

Mice

Mice, Inbred Strains

Molecular Sequence Data

Muridae

Muscular Dystrophy, Animal

Mutation

Source

Open in PubMed

Identifiers

PMID: 7613034
DOI: 10.1007/BF00352416

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-7613034-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

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