Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1996 | 1 |
2000 | 1 |
2001 | 1 |
2007 | 2 |
2024 | 0 |
PubMed (cited) for id: 601316
5 results
Results by year
Filters applied: . Clear all
Page 1
A novel splice site mutation in EYA4 causes DFNA10 hearing loss.
Am J Med Genet A. 2007 Jul 15;143A(14):1599-604. doi: 10.1002/ajmg.a.31860.
Am J Med Genet A. 2007.
PMID: 17568404
Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain.
Makishima T, Madeo AC, Brewer CC, Zalewski CK, Butman JA, Sachdev V, Arai AE, Holbrook BM, Rosing DR, Griffith AJ.
Makishima T, et al.
Am J Med Genet A. 2007 Jul 15;143A(14):1592-8. doi: 10.1002/ajmg.a.31793.
Am J Med Genet A. 2007.
PMID: 17567890
Item in Clipboard
Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus.
Wayne S, Robertson NG, DeClau F, Chen N, Verhoeven K, Prasad S, Tranebjärg L, Morton CC, Ryan AF, Van Camp G, Smith RJ.
Wayne S, et al.
Hum Mol Genet. 2001 Feb 1;10(3):195-200. doi: 10.1093/hmg/10.3.195.
Hum Mol Genet. 2001.
PMID: 11159937
Item in Clipboard
Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment.
Verhoeven K, Fagerheim T, Prasad S, Wayne S, De Clau F, Balemans W, Verstreken M, Schatteman I, Solem B, Van de Heyning P, Tranebjärg L, Smith RJ, Van Camp G.
Verhoeven K, et al.
Hum Genet. 2000 Jul;107(1):7-11. doi: 10.1007/s004390000319.
Hum Genet. 2000.
PMID: 10982027
Item in Clipboard
A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6.
O'Neill ME, Marietta J, Nishimura D, Wayne S, Van Camp G, Van Laer L, Negrini C, Wilcox ER, Chen A, Fukushima K, Ni L, Sheffield VC, Smith RJ.
O'Neill ME, et al.
Hum Mol Genet. 1996 Jun;5(6):853-6. doi: 10.1093/hmg/5.6.853.
Hum Mol Genet. 1996.
PMID: 8776603
Item in Clipboard
Cite
Cite