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Year | Number of Results |
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1999 | 1 |
2000 | 1 |
2006 | 1 |
2014 | 1 |
2024 | 0 |
PubMed (cited) for id: 603622
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c.G2114A MYH9 mutation (DFNA17) causes non-syndromic autosomal dominant hearing loss in a Brazilian family.
Genet Mol Biol. 2014 Oct;37(4):616-21. doi: 10.1590/S1415-47572014005000025. Epub 2014 Nov 14.
Genet Mol Biol. 2014.
PMID: 25505834
Free PMC article.
Cochlear implants for DFNA17 deafness.
Hildebrand MS, de Silva MG, Gardner RJ, Rose E, de Graaf CA, Bahlo M, Dahl HH.
Hildebrand MS, et al.
Laryngoscope. 2006 Dec;116(12):2211-5. doi: 10.1097/01.mlg.0000242089.72880.f8.
Laryngoscope. 2006.
PMID: 17146397
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Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9.
Lalwani AK, Goldstein JA, Kelley MJ, Luxford W, Castelein CM, Mhatre AN.
Lalwani AK, et al.
Am J Hum Genet. 2000 Nov;67(5):1121-8. doi: 10.1016/S0002-9297(07)62942-5. Epub 2000 Oct 9.
Am J Hum Genet. 2000.
PMID: 11023810
Free PMC article.
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A new locus for nonsyndromic hereditary hearing impairment, DFNA17, maps to chromosome 22 and represents a gene for cochleosaccular degeneration.
Lalwani AK, Luxford WM, Mhatre AN, Attaie A, Wilcox ER, Castelein CM.
Lalwani AK, et al.
Am J Hum Genet. 1999 Jan;64(1):318-23. doi: 10.1086/302216.
Am J Hum Genet. 1999.
PMID: 9915977
Free PMC article.
No abstract available.
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A five-generation family with late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration.
Lalwani AK, Linthicum FH, Wilcox ER, Moore JK, Walters FC, San Agustin TB, Mislinski J, Miller MR, Sinninger Y, Attaie A, Luxford WM.
Lalwani AK, et al.
Audiol Neurootol. 1997 May-Jun;2(3):139-54. doi: 10.1159/000259237.
Audiol Neurootol. 1997.
PMID: 9390828
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