Mitochondrial mutations and hearing loss: Paradigm for mitochondrial genetics

被引：62

作者：

Fischel-Ghodsian, N

机构：

[1] Cedars Sinai Med Ctr, Ahmanson Dept Pediat, Steven Spielberg Pediat Res Ctr, Los Angeles, CA 90048 USA

[2] Univ Calif Los Angeles, Sch Med, Los Angeles, CA USA

来源：

AMERICAN JOURNAL OF HUMAN GENETICS | 1998年 / 62卷 / 01期

关键词：

D O I：

10.1086/301695

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：15 / 19

页数：5

共 31 条

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[5] Two large Spanish pedigrees with nonsyndromic sensorineural deafness and the mtDNA mutation at nt 1555 in the 12S rRNA gene: Evidence of heteroplasmy
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[6] Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment with aminoglycosides
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[7] MITOCHONDRIAL MUTATION ASSOCIATED WITH NONSYNDROMIC DEAFNESS
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[8] Temporal bone analysis of patients with presbycusis reveals high frequency of mitochondrial mutations
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[9] Mitochondrial gene mutation is a significant predisposing factor in aminoglycoside ototoxicity
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[J]. AMERICAN JOURNAL OF OTOLARYNGOLOGY, 1997, 18 (03) : 173 - 178
[10] MITOCHONDRIAL RIBOSOMAL-RNA GENE MUTATION IN A PATIENT WITH SPORADIC AMINOGLYCOSIDE OTOTOXICITY
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[J]. AMERICAN JOURNAL OF OTOLARYNGOLOGY, 1993, 14 (06) : 399 - 403

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