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Article

Missplicing resulting from a short deletion in the reelin gene causes reeler-like neuronal disorders in the mutant shaking rat Kawasaki.

The Journal of comparative neurology - 25 Aug 2003

Kikkawa Satoshi, Yamamoto Tatsuro, Misaki Kazuyo, Ikeda Yayoi, Okado Haruo, Ogawa Masaharu, Woodhams Peter L, Terashima Toshio

Abstract excerpt

The shaking rat Kawasaki (SRK) is an autosomal recessive mutant that exhibits reeler-like abnormal locomotor behaviors. The murine reeler mutants arise from several mutations in the specific gene called reelin, which result in defects of Reelin expression or secretion in the cerebral cortex and o...

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Source

Identifiers

PMID: 12820163
DOI: 10.1002/cne.10761

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-12820163-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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Missplicing resulting from a short deletion in the reelin gene causes reeler-like neuronal disorders in the mutant shaking rat Kawasaki.PMID 12820163Read ↗

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