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Year | Number of Results |
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1995 | 1 |
1998 | 2 |
2002 | 1 |
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2024 | 0 |
PubMed (OMIM) for id: 322209
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Page 1
Nonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4).
Am J Hum Genet. 2004 Apr;74(4):770-6. doi: 10.1086/383285. Epub 2004 Mar 10.
Am J Hum Genet. 2004.
PMID: 15015131
Free PMC article.
A novel myosin heavy chain gene in human chromosome 19q13.3.
Leal A, Endele S, Stengel C, Huehne K, Loetterle J, Barrantes R, Winterpacht A, Rautenstrauss B.
Leal A, et al.
Gene. 2003 Jul 17;312:165-71. doi: 10.1016/s0378-1119(03)00613-9.
Gene. 2003.
PMID: 12909352
Item in Clipboard
Second family with hearing impairment linked to 19q13 and refined DFNA4 localisation.
Mirghomizadeh F, Bardtke B, Devoto M, Pfister M, Oeken J, König E, Vitale E, Riccio A, De Rienzo A, Zenner HP, Blin N.
Mirghomizadeh F, et al.
Eur J Hum Genet. 2002 Feb;10(2):95-9. doi: 10.1038/sj.ejhg.5200769.
Eur J Hum Genet. 2002.
PMID: 11938438
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Characterization of the human mitochondrial ribosomal S12 gene.
Johnson DF, Hamon M, Fischel-Ghodsian N.
Johnson DF, et al.
Genomics. 1998 Sep 15;52(3):363-8. doi: 10.1006/geno.1998.5448.
Genomics. 1998.
PMID: 9790755
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Chromosomal locations of three human nuclear genes (RPSM12, TUFM, and AFG3L1) specifying putative components of the mitochondrial gene expression apparatus.
Shah ZH, Migliosi V, Miller SC, Wang A, Friedman TB, Jacobs HT.
Shah ZH, et al.
Genomics. 1998 Mar 15;48(3):384-8. doi: 10.1006/geno.1997.5166.
Genomics. 1998.
PMID: 9545647
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Linkage of a gene for dominant non-syndromic deafness to chromosome 19.
Chen AH, Ni L, Fukushima K, Marietta J, O'Neill M, Coucke P, Willems P, Smith RJ.
Chen AH, et al.
Hum Mol Genet. 1995 Jun;4(6):1073-6. doi: 10.1093/hmg/4.6.1073.
Hum Mol Genet. 1995.
PMID: 7655461
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