(Q35433389)

8 August 2017

title

Prevalence of mitochondrial gene mutations among hearing impaired patients (English)

1 reference

8 August 2017

Usami S

1

1 reference

8 August 2017

Abe S

2

1 reference

8 August 2017

Akita J

3

1 reference

8 August 2017

Namba A

4

1 reference

8 August 2017

Shinkawa H

5

1 reference

8 August 2017

Ishii M

6

1 reference

8 August 2017

Iwasaki S

7

1 reference

8 August 2017

Hoshino T

8

1 reference

8 August 2017

Ito J

9

1 reference

8 August 2017

Doi K

10

1 reference

8 August 2017

Kubo T

11

1 reference

8 August 2017

Nakagawa T

12

1 reference

8 August 2017

Komiyama S

13

1 reference

8 August 2017

Tono T

14

1 reference

8 August 2017

Komune S

15

1 reference

8 August 2017

language of work or name

English

0 references

publication date

1 January 2000

1 reference

Journal of Medical Genetics

8 August 2017

published in

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8 August 2017

volume

37

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8 August 2017

issue

1

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8 August 2017

page(s)

38-40

1 reference

Cochlear implantation in a patient with profound hearing loss with the A1555G mitochondrial mutation.

8 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734443

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734443

Mitochondrial A7445G mutation in two pedigrees with palmoplantar keratoderma and deafness

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734443

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734443

Multiple origins of a mitochondrial mutation conferring deafness.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734443

Mitochondrial mutation associated with nonsyndromic deafness

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734443

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734443

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734443

Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734443

Rapid mass screening method and counseling for the 1555A-->G mitochondrial mutation

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734443

Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutation

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734443

Isepamicin sulfate-induced sensorineural hearing loss in patients with the 1555 A-->G mitochondrial mutation

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734443

Mitochondrial gene mutation is a significant predisposing factor in aminoglycoside ototoxicity

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734443

A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734443

A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafness.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734443

26 September 2018

Identifiers

DOI

10.1136/JMG.37.1.38

1 reference

8 August 2017

1 reference

8 August 2017

1 reference