(Q37072839)

18 August 2017

A rapid method for detection of five known mutations associated with aminoglycoside-induced deafness (English)

1 reference

18 August 2017

1 reference

Lize van der Merwe

7

0 references

Soraya Bardien

1

object named as

Soraya Bardien

1 reference

18 August 2017

Hannique Human

2

1 reference

18 August 2017

Tashneem Harris

3

1 reference

18 August 2017

Gwynneth Hefke

4

1 reference

18 August 2017

Rene Veikondis

5

1 reference

18 August 2017

H Simon Schaaf

6

1 reference

18 August 2017

John H Greinwald

8

1 reference

18 August 2017

Johan Fagan

9

1 reference

18 August 2017

Greetje de Jong

10

1 reference

18 August 2017

13 January 2009

1 reference

18 August 2017

1 reference

18 August 2017

10

1 reference

18 August 2017

2

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2350-10-2

18 August 2017

0 references

cites work

Mitochondrial deafness alleles confer misreading of the genetic code

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2630920

Mitochondrial non-syndromic sensorineural hearing loss: a clinical, audiological and pathological study from Italy, and revision of the literature

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2630920

Mitochondrial rRNA and tRNA and hearing function

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2630920

A new method for analysis of mitochondrial DNA point mutations and assess levels of heteroplasmy

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2630920

Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2630920

Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2630920

Primer3 on the WWW for general users and for biologist programmers

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2630920

Familial aggregation of streptomycin ototoxicity: autosomal dominant inheritance?

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2630920

Genetic aspects of antibiotic induced deafness: mitochondrial inheritance

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2630920

Carrier frequency of the 35delG and A1555G deafness mutations in the Argentinean population. Impact on the newborn hearing screening.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2630920

Maternally inherited non-syndromic hearing loss associated with mitochondrial 12S rRNA A827G mutation in a Chinese family.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2630920

Genetic features, clinical phenotypes, and prevalence of sensorineural hearing loss associated with the 961delT mitochondrial mutation

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2630920

A novel mitochondrial mutation, 1556C --> T, in a Japanese patient with streptomycin-induced tinnitus

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2630920

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

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2630920

A novel mitochondrial 12SrRNA point mutation in parkinsonism, deafness, and neuropathy.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2630920

Rapid identification of an A1555G mutation in human mitochondrial DNA implicated in aminoglycoside-induced ototoxicity.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2630920

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

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2630920

Streptomycin ototoxicity in the unborn child.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2630920

Multidrug-resistant tuberculosis

4 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1471-2350-10-2

Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside induced deafness

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19144107

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2350-10-2

1 reference

Dimensions Publication ID

18 August 2017

0 references

1 reference

18 August 2017

1 reference