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Article

Human homologue of a gene mutated in the slow Wallerian degeneration (C57BL/Wld(s)) mouse.

Gene - 6 Feb 2002

Fernando F Shama, Conforti Laura, Tosi Sabrina, Smith A David, Coleman Michael P

Abstract excerpt

The slow Wallerian degeneration mouse (C57BL/Wld(s)) is a mutant strain of mouse, with the unique phenotype of prolonged survival of the distal axon following axotomy. The causative mutation is an 85 kb tandem triplication on distal mouse chromosome 4. The dominant slow Wallerian degeneration phenotype is conferred by a hybrid gene within the triplication, comprising a gene of previously unknown function,...

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Share to Blotting, Northern
Share to Chromosomes, Human, Pair 1
Share to Cloning, Molecular

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to In Situ Hybridization, Fluorescence

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Share to Sequence Homology, Amino Acid

Source

Identifiers

PMID: 11891043
DOI: 10.1016/s0378-1119(02)00394-3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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