(Q44122843)

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Age of onset possibly associated with the degree of heteroplasmy in two male siblings with diabetes mellitus having an A to G transition at 3243 of mitochondrial DNA.

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

Age of onset possibly associated with the degree of heteroplasmy in two male siblings with diabetes mellitus having an A to G transition at 3243 of mitochondrial DNA. (English)

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

mitochondrial DNA

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1 reference

based on heuristic

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based on heuristic

author name string

Kato Y

1

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

Miura Y

2

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

Inagaki A

3

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

Itatsu T

4

1 reference

Europe PubMed Central

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30 November 2017

Oiso Y

5

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

publication date

1 September 2002

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Europe PubMed Central

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30 November 2017

Diabetic Medicine

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Europe PubMed Central

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30 November 2017

19

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Europe PubMed Central

PubMed publication ID

30 November 2017

9

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

784-786

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu(UUR) gene mutation

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2002.00777.X

21 January 2018

Sequence of a variant thyroxine-binding globulin (TBG) in a family with partial TBG deficiency in Japanese (TBG-PDJ).

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2002.00777.X

21 January 2018

Sequence and organization of the human mitochondrial genome

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2002.00777.X

21 January 2018

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2002.00777.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2002.00777.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2002.00777.X

21 January 2018

Prevalence and clinical characterization of Japanese diabetes mellitus with an A-to-G mutation at nucleotide 3243 of the mitochondrial tRNA(Leu(UUR)) gene.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2002.00777.X

21 January 2018

Clinical and laboratory characteristics in the families with diabetes and a mitochondrial tRNA(LEU(UUR)) gene mutation.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2002.00777.X

21 January 2018

Mitochondrial genetics: a paradigm for aging and degenerative diseases?

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2002.00777.X

21 January 2018

Prevalence of maternally inherited diabetes and deafness in diabetic populations in the Netherlands

1 reference

https://api.crossref.org/works/10.1046%2FJ.1464-5491.2002.00777.X

21 January 2018

Identifiers

10.1046/J.1464-5491.2002.00777.X

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

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