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Article

Effects of shaker-1 mutations on myosin-VIIa protein and mRNA expression.

Cell motility and the cytoskeleton - 1 Jan 1997

Hasson T, Walsh J, Cable J, Mooseker M S, Brown S D, Steel K P

Abstract excerpt

Numerous mammalian diseases have been found to be due to mutations in components of the actin cytoskeleton. Recently, mutations in the gene for an unconventional myosin, myosin-VIIa, were found to be the basis for the deafness and vestibular dysfunction observed in shaker-1 (sh1) mice and for a human deafness-blindness syndrome, Usher syndrome type 1B. Seven alleles of sh1 mice were analyzed to assess the affects...

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Identifiers

PMID: 9186010
DOI: 10.1002/(SICI)1097-0169(1997)37:2<127::AID-CM5>3.0.CO;2-5

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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