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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2009 | 2 |
2010 | 1 |
2024 | 0 |
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Mutations in the first MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss.
Laryngoscope. 2009 Apr;119(4):727-33. doi: 10.1002/lary.20116.
Laryngoscope. 2009.
PMID: 19274735
Free PMC article.
A novel mutation adjacent to the Bth mouse mutation in the TMC1 gene makes this mouse an excellent model of human deafness at the DFNA36 locus.
Yang T, Kahrizi K, Bazazzadeghan N, Meyer N, Najmabadi H, Smith RJ.
Yang T, et al.
Clin Genet. 2010 Apr;77(4):395-8. doi: 10.1111/j.1399-0004.2009.01338.x.
Clin Genet. 2010.
PMID: 20447146
Free PMC article.
No abstract available.
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Multi-granularity Parallel Computing in a Genome-Scale Molecular Evolution Application.
Walters JD, Bair TB, Braun TA, Scheetz TE, Robinson JP, Casavant TL.
Walters JD, et al.
J Supercomput. 2009 Jan 1;5698:49-59. doi: 10.1007/978-3-642-03275-2_6.
J Supercomput. 2009.
PMID: 21841894
Free PMC article.
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