Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 13

1.

Maternally transmitted late-onset non-syndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial tRNAHis gene.

Yan X, Wang X, Wang Z, Sun S, Chen G, He Y, Mo JQ, Li R, Jiang P, Lin Q, Sun M, Li W, Bai Y, Zhang J, Zhu Y, Lu J, Yan Q, Li H, Guan MX.

J Med Genet. 2011 Oct;48(10):682-90. doi: 10.1136/jmedgenet-2011-100219.

PMID:
21931169
[PubMed - indexed for MEDLINE]
2.

[Modifier factors influencing the phenotypic manifestation of the deafness associated mitochondrial DNA mutations].

YANG AF, ZHENG J, LV JX, GUAN MX.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Apr;28(2):165-71. doi: 10.3760/cma.j.issn.1003-9406.2011.02.010. Review. Chinese.

PMID:
21462128
[PubMed - indexed for MEDLINE]
3.

Mitochondrial deafness.

Kokotas H, Petersen MB, Willems PJ.

Clin Genet. 2007 May;71(5):379-91. Review.

PMID:
17489842
[PubMed - indexed for MEDLINE]
4.

The genetic bases for non-syndromic hearing loss among Chinese.

Ouyang XM, Yan D, Yuan HJ, Pu D, Du LL, Han DY, Liu XZ.

J Hum Genet. 2009 Mar;54(3):131-40. doi: 10.1038/jhg.2009.4. Epub 2009 Feb 6. Review.

PMID:
19197336
[PubMed - indexed for MEDLINE]
5.

The role of mitochondrial DNA mutations in hearing loss.

Ding Y, Leng J, Fan F, Xia B, Xu P.

Biochem Genet. 2013 Aug;51(7-8):588-602. doi: 10.1007/s10528-013-9589-6. Epub 2013 Apr 21. Review.

PMID:
23605717
[PubMed - indexed for MEDLINE]
6.

Hereditary non-syndromic sensorineural hearing loss: transforming silence to sound.

Schrijver I.

J Mol Diagn. 2004 Nov;6(4):275-84. Review.

PMID:
15507665
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

c-Ret-mediated hearing losses.

Ohgami N, Tamura H, Ohgami K, Iida M, Yajima I, Kumasaka MY, Goto Y, Sone M, Nakashima T, Kato M.

Int J Clin Exp Pathol. 2012;5(1):23-8. Epub 2012 Jan 1. Review.

PMID:
22295143
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Vestibular function in families with inherited autosomal dominant hearing loss.

Street VA, Kallman JC, Strombom PD, Bramhall NF, Phillips JO.

J Vestib Res. 2008;18(1):51-8. Review.

PMID:
18776598
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Nuclear factors: roles related to mitochondrial deafness.

Luo LF, Hou CC, Yang WX.

Gene. 2013 May 15;520(2):79-89. doi: 10.1016/j.gene.2013.03.041. Epub 2013 Mar 17. Review.

PMID:
23510774
[PubMed - indexed for MEDLINE]
10.

An overview of hereditary hearing loss.

Bayazit YA, Yilmaz M.

ORL J Otorhinolaryngol Relat Spec. 2006;68(2):57-63. Epub 2006 Jan 20. Review.

PMID:
16428895
[PubMed - indexed for MEDLINE]
Free Article
11.

Hearing loss and PRPS1 mutations: Wide spectrum of phenotypes and potential therapy.

Liu XZ, Xie D, Yuan HJ, de Brouwer AP, Christodoulou J, Yan D.

Int J Audiol. 2013 Jan;52(1):23-8. doi: 10.3109/14992027.2012.736032. Epub 2012 Nov 28. Review.

PMID:
23190330
[PubMed - indexed for MEDLINE]
12.

Inheritance patterns of progressive hearing loss in laboratory strains of mice.

Noben-Trauth K, Johnson KR.

Brain Res. 2009 Jun 24;1277:42-51. doi: 10.1016/j.brainres.2009.02.012. Epub 2009 Feb 21. Review.

PMID:
19236853
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

High-throughput sequencing to decipher the genetic heterogeneity of deafness.

Brownstein Z, Bhonker Y, Avraham KB.

Genome Biol. 2012 May 29;13(5):245. doi: 10.1186/gb-2012-13-5-245. Review.

PMID:
22647651
[PubMed - indexed for MEDLINE]
Free PMC Article

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk