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Article

Genetic mapping of the whirler mutation.

Mammalian genome : official journal of the International Mammalian Genome Society - 1 May 1999

Rogers M J, Fleming J, Kiernan B W, Mburu P, Varela A, Brown S D, Steel K P

Abstract excerpt

The whirler (wi) mutation on mouse Chromosome (Chr) 4 results in an autosomal recessive neuroepithelial deafness and vestibular dysfunction exhibited as a characteristic shaker-waltzer behavior (deafness, circling, and head-bobbing). We have constructed a genetic linkage map across the wi region in both an interspecific [(wi/wi x CAST/Ei)F1 x wi/wi] backcross (n = 817) and an intraspecific [(wi/wi x CBA/Ca)F1 x...

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Identifiers

PMID: 10337627
DOI: 10.1007/s003359901032

Genes

CAST

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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.

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