(Q46500420)

22 December 2017

title

Genetic susceptibility to aminoglycoside ototoxicity: how many are at risk? (English)

1 reference

22 December 2017

1 reference

Hsiao-Yuan Tang

1

1 reference

22 December 2017

Eldridge Hutcheson

2

1 reference

22 December 2017

Susan Neill

3

1 reference

22 December 2017

Margaret Drummond-Borg

4

1 reference

22 December 2017

Michael Speer

5

1 reference

22 December 2017

Raye Lynn Alford

6

1 reference

22 December 2017

language of work or name

English

0 references

publication date

1 September 2002

1 reference

22 December 2017

published in

Genetics in Medicine

1 reference

22 December 2017

volume

4

1 reference

22 December 2017

issue

5

1 reference

22 December 2017

page(s)

336-345

1 reference

22 December 2017

https://scigraph.springernature.com/pub.10.1097/00125817-200209000-00004

exact match

0 references

cites work

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

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

A molecular basis for human hypersensitivity to aminoglycoside antibiotics

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

Inherited susceptibility to aminoglycoside ototoxicity: genetic heterogeneity and clinical implications

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

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/10.1097%2F00125817-200209000-00004

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/10.1097%2F00125817-200209000-00004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

Prevalence of mitochondrial gene mutations among hearing impaired patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

The A1555G mutation in the 12S rRNA gene of human mtDNA: recurrent origins and founder events in families affected by sensorineural deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

The emerging tree of West Eurasian mtDNAs: a synthesis of control-region sequences and RFLPs

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

Human mtDNA haplogroups associated with high or reduced spermatozoa motility

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

Mitochondrial DNA and human evolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

U.S. newborn screening policy dilemmas for the twenty-first century

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

Maternally inherited cardiomyopathy: an atypical presentation of the mtDNA 12S rRNA gene A1555G mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200209000-00004

10.1097/00125817-200209000-00004

21 January 2018

Identifiers

DOI

1 reference

22 December 2017

Dimensions Publication ID

0 references

1 reference

22 December 2017