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Year | Number of Results |
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2003 | 1 |
2013 | 1 |
2014 | 1 |
2024 | 0 |
PubMed (cited) for id: 613865
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Utilizing ethnic-specific differences in minor allele frequency to recategorize reported pathogenic deafness variants.
Am J Hum Genet. 2014 Oct 2;95(4):445-53. doi: 10.1016/j.ajhg.2014.09.001. Epub 2014 Sep 25.
Am J Hum Genet. 2014.
PMID: 25262649
Free PMC article.
Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: a cross-sectional, multi-center next-generation sequencing study.
Mutai H, Suzuki N, Shimizu A, Torii C, Namba K, Morimoto N, Kudoh J, Kaga K, Kosaki K, Matsunaga T.
Mutai H, et al.
Orphanet J Rare Dis. 2013 Oct 28;8:172. doi: 10.1186/1750-1172-8-172.
Orphanet J Rare Dis. 2013.
PMID: 24164807
Free PMC article.
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Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss.
Liu XZ, Ouyang XM, Xia XJ, Zheng J, Pandya A, Li F, Du LL, Welch KO, Petit C, Smith RJ, Webb BT, Yan D, Arnos KS, Corey D, Dallos P, Nance WE, Chen ZY.
Liu XZ, et al.
Hum Mol Genet. 2003 May 15;12(10):1155-62. doi: 10.1093/hmg/ddg127.
Hum Mol Genet. 2003.
PMID: 12719379
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