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Article

Identification of break points in mutated PMP22 gene in a new Trembler (Tr-Ncnp) mouse.

Neuroscience - 1 Jan 1999

Sakai Y, Nakabayashi O, Kikuchi T, Wada K

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 10363833
DOI: 10.1016/s0306-4522(98)00402-3

Genes

PMP22

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

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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Identification of break points in mutated PMP22 gene in a new Trembler (Tr-Ncnp) mouse.PMID 10363833Read ↗

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Trembler mouse carries a point mutation in a myelin gene.Semantic proximity Read ↗

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PMP22 Carrying the Trembler or Trembler-J Mutation Is Intracellularly Retained in Myelinating Schwann CellsSemantic proximity Read ↗

Genetic alterations in the mouse myelin basic proteins result in a range of dysmyelinating disorders.Semantic proximity Read ↗

Molecular characterization of the murine mutation myelin deficient.Semantic proximity Read ↗

Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy.Semantic proximity Read ↗

NEW SPLOTCH ALLELES IN THE MOUSE.Semantic proximity Read ↗

Identification of a new Pmp22 mouse mutant and trafficking analysis of a Pmp22 allelic series suggesting that protein aggregates may be protective in Pmp22-associated peripheral neuropathy.Semantic proximity Read ↗

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