(Q28379261)

2 July 2017

Familial streptomycin ototoxicity in a South African family: a mitochondrial disorder (English)

1 reference

2 July 2017

0 references

1 reference

1 reference

Gardner JC

1

1 reference

2 July 2017

Goliath R

2

1 reference

2 July 2017

Viljoen D

3

1 reference

2 July 2017

Sellars S

4

1 reference

2 July 2017

Cortopassi G

5

1 reference

2 July 2017

Hutchin T

6

1 reference

2 July 2017

Greenberg J

7

1 reference

2 July 2017

Beighton P

8

1 reference

2 July 2017

language of work or name

English

0 references

publication date

1 November 1997

1 reference

Journal of Medical Genetics

2 July 2017

1 reference

2 July 2017

34

1 reference

2 July 2017

904-906

1 reference

2 July 2017

11

1 reference

Familial aggregation of streptomycin ototoxicity: autosomal dominant inheritance?

2 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051117

Multiple origins of a mitochondrial mutation conferring deafness.

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051117

A molecular basis for human hypersensitivity to aminoglycoside antibiotics

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051117

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=1051117

Sensorineural deafness inherited as a tissue specific mitochondrial disorder

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051117

Unique inheritance of streptomycin-induced deafness

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051117

Non-syndromic deafness associated with a mutation and a polymorphism in the mitochondrial 12S ribosomal RNA gene in a large Zairean pedigree

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051117

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

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051117

Childhood deafness in southern Africa. An aetiological survey of 3,064 deaf children.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051117

A molecular and cellular hypothesis for aminoglycoside-induced deafness

27 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9391883

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.34.11.904

1 reference

2 July 2017

0 references

1 reference