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In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairment.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 16, p. 3075
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- Publication type:
- Article
Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing loss.
- Published in:
- Nature Genetics, 2009, v. 41, n. 5, p. 609, doi. 10.1038/ng.355
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- Publication type:
- Article