Mapping of the gracile axonal dystrophy (gad) gene to a region between D5Mit197 and D5Mit113 on proximal mouse chromosome 5.

doi:10.1006/geno.1995.1091

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Article

Mapping of the gracile axonal dystrophy (gad) gene to a region between D5Mit197 and D5Mit113 on proximal mouse chromosome 5.

Genomics - 10 Jun 1995

Suh J G, Yamanishi T, Matsui K, Tanaka K, Wada K

Abstract excerpt

The gracile axonal dystrophy (gad) mouse, which shows hereditary sensory ataxia and motor paresis, has been morphologically characterized by the dying back type of axonal degeneration in the nerve terminals of dorsal root ganglion cells and motor neurons. In the present study, using an intraspecific backcross between gad and C57BL/6J mice, the gracile axonal dystrophy (gad) gene was mapped to a region between...

Topics

Alleles
Animals
Chromosome Mapping
Chromosomes, Artificial, Yeast
Chromosomes, Human, Pair 4
Crosses, Genetic
Female
Genetic Linkage
Genetic Markers
Humans
Male

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Mice

Mice, Inbred C57BL

Mice, Neurologic Mutants

Mutation

Species Specificity

Spinocerebellar Degenerations

Source

Open in PubMed

Identifiers

PMID: 7558041
DOI: 10.1006/geno.1995.1091

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-7558041-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

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

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