(Q50501379)

14 March 2018

title

Sensorineural hearing loss and the 1555G mitochondrial DNA mutation. (English)

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14 March 2018

sensorineural hearing loss

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1 reference

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Hutchin T

1

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14 March 2018

language of work or name

English

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publication date

1 January 1999

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14 March 2018

number of pages

5

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based on heuristic

inferred from page(s)

published in

Acta Oto-Laryngologica

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14 March 2018

volume

119

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14 March 2018

issue

1

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14 March 2018

page(s)

48-52

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14 March 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1080%2F00016489950181927

A molecular basis for human hypersensitivity to aminoglycoside antibiotics

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00016489950181927

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00016489950181927

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00016489950181927

Genetic and clinical features of sensorineural hearing loss associated with the 1555 mitochondrial mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00016489950181927

Familial streptomycin ototoxicity in a South African family: a mitochondrial disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00016489950181927

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00016489950181927

Audiovestibular findings in patients with deafness caused by a mitochondrial susceptibility mutation and precipitated by an inherited nuclear mutation or aminoglycosides.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00016489950181927

Sensorineural deafness inherited as a tissue specific mitochondrial disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00016489950181927

Non-Mendelian mitochondrial inheritance as a cause of progressive genetic sensorineural hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00016489950181927

Interaction of antibiotics with functional sites in 16S ribosomal RNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00016489950181927

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00016489950181927

10.1080/00016489950181927

21 January 2018

Identifiers

DOI

1 reference

14 March 2018

PubMed ID

10219384

1 reference

14 March 2018