Aminoglycoside-induced deafness associated with the mitochondrial DNA mutation A1555G. (Q39459080)

12 September 2017

Aminoglycoside-induced deafness associated with the mitochondrial DNA mutation A1555G. (English)

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12 September 2017

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Shohat M

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12 September 2017

Fischel-Ghodsian N

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12 September 2017

Legum C

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Halpern GJ

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1 January 1999

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American Journal of Otolaryngology

12 September 2017

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12 September 2017

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A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: evidence from pedigree segregation analysis

12 September 2017

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https://api.crossref.org/works/10.1016%2FS0196-0709%2899%2990054-6

7 January 2021

Genetic aspects of antibiotic induced deafness: mitochondrial inheritance

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https://api.crossref.org/works/10.1016%2FS0196-0709%2899%2990054-6

7 January 2021

Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity.

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https://api.crossref.org/works/10.1016%2FS0196-0709%2899%2990054-6

7 January 2021

Sensorineural deafness inherited as a tissue specific mitochondrial disorder

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https://api.crossref.org/works/10.1016%2FS0196-0709%2899%2990054-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0196-0709%2899%2990054-6

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%2990054-6

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.

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https://api.crossref.org/works/10.1016%2FS0196-0709%2899%2990054-6

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%2990054-6

7 January 2021

Mitochondrial DNA mutation at nucleotide 1555 in a patient with bilateral sensorineural hearing loss of unknown etiology.

1 reference

https://api.crossref.org/works/10.1016%2FS0196-0709%2899%2990054-6

7 January 2021

A molecular basis for human hypersensitivity to aminoglycoside antibiotics

1 reference

https://api.crossref.org/works/10.1016%2FS0196-0709%2899%2990054-6

7 January 2021

Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0196-0709%2899%2990054-6

7 January 2021

Mutant mtDNA at 1555 A to G in 12S rRNA gene and hypersusceptibility of mitochondrial translation to streptomycin can be co-transferred to rho 0 HeLa cells

1 reference

https://api.crossref.org/works/10.1016%2FS0196-0709%2899%2990054-6

7 January 2021

10.1016/S0196-0709(99)90054-6

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12 September 2017

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