Genetic aspects of antibiotic induced deafness: mitochondrial inheritance (Q33596549)

28 July 2017

title

Genetic aspects of antibiotic induced deafness: mitochondrial inheritance (English)

1 reference

28 July 2017

1 reference

Hu DN

1

1 reference

28 July 2017

Qui WQ

2

1 reference

28 July 2017

Wu BT

3

1 reference

28 July 2017

Fang LZ

4

1 reference

28 July 2017

Zhou F

5

1 reference

28 July 2017

Gu YP

6

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28 July 2017

Zhang QH

7

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28 July 2017

Yan JH

8

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28 July 2017

Ding YQ

9

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28 July 2017

Wong H

10

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28 July 2017

language of work or name

English

0 references

publication date

1 February 1991

1 reference

Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

28

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28 July 2017

issue

2

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28 July 2017

page(s)

79-83

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Altered ribosomal RNA genes in mitochondria from mammalian cells with chloramphenicol resistance

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016772

Sequence and organization of the human mitochondrial genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016772

Familial aggregation of streptomycin ototoxicity: autosomal dominant inheritance?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016772

Concordance for drug-induced aplastic anemia in identical twins

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016772

Familial occurrence of drug-induced hearing loss.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016772

Familial incidence of streptomycin hearing loss and hereditary weakness of the cochlea.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016772

Deletions of mitochondrial DNA in Kearns-Sayre syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016772

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016772

Ototoxicity with Children caused by Streptomycin

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016772

Mitochondrial inheritance and disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016772

FAMILIAL SENSITIVITY TO STREPTOMYCIN.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016772

Streptomycin ototoxicity in the unborn child.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016772

Cytoplasmic transfer of chloramphenicol resistance in a human cell line

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2002491

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Mitochondrial inheritance in a mitochondrially mediated disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2002491

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.28.2.79

1 reference

28 July 2017

1 reference

28 July 2017

1 reference