(Q41664813)

6 October 2017

title

Inherited susceptibility to aminoglycoside ototoxicity: genetic heterogeneity and clinical implications (English)

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6 October 2017

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Casano RA

1

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6 October 2017

Johnson DF

2

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6 October 2017

Bykhovskaya Y

3

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6 October 2017

Torricelli F

4

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6 October 2017

Bigozzi M

5

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6 October 2017

Fischel-Ghodsian N

6

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6 October 2017

publication date

1 May 1999

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American Journal of Otolaryngology

6 October 2017

published in

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6 October 2017

volume

20

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6 October 2017

issue

3

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6 October 2017

page(s)

151-156

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Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness

6 October 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0196-0709%2899%2990062-5

7 January 2021

A molecular basis for human hypersensitivity to aminoglycoside antibiotics

1 reference

https://api.crossref.org/works/10.1016%2FS0196-0709%2899%2990062-5

7 January 2021

Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity

1 reference

https://api.crossref.org/works/10.1016%2FS0196-0709%2899%2990062-5

7 January 2021

Two large Spanish pedigrees with nonsyndromic sensorineural deafness and the mtDNA mutation at nt 1555 in the 12s rRNA gene: evidence of heteroplasmy.

1 reference

https://api.crossref.org/works/10.1016%2FS0196-0709%2899%2990062-5

7 January 2021

Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides

1 reference

https://api.crossref.org/works/10.1016%2FS0196-0709%2899%2990062-5

7 January 2021

Mitochondrial gene mutation is a significant predisposing factor in aminoglycoside ototoxicity.

1 reference

https://api.crossref.org/works/10.1016%2FS0196-0709%2899%2990062-5

7 January 2021

Mitochondrial mutation associated with nonsyndromic deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0196-0709%2899%2990062-5

7 January 2021

Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0196-0709%2899%2990062-5

7 January 2021

Length mutations in human mitochondrial DNA: direct sequencing of enzymatically amplified DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0196-0709%2899%2990062-5

7 January 2021

Specific binding of aminoglycosides to a human rRNA construct based on a DNA polymorphism which causes aminoglycoside-induced deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0196-0709%2899%2990062-5

7 January 2021

10.1016/S0196-0709(99)90062-5

Identifiers

DOI

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6 October 2017

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