(Q57420556)

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A Case of a De Novo A3243G Mutation in Mitochondrial DNA in a Patient with Diabetes and Deafness

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A Case of a De Novo A3243G Mutation in Mitochondrial DNA in a Patient with Diabetes and Deafness (English)

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1 reference

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J.A. Maassen

1

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S. Biberoglu

series ordinal

2

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L.M. ’t Hart

series ordinal

3

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E. Bakker

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4

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P. de Knijff

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5

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publication date

January 2002

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published in

Archives of Physiology and Biochemistry

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volume

110

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issue

3

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page(s)

186-188

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cites work

Mitochondrial DNA polymorphism in a maternal lineage of Holstein cows

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reference URL

https://api.crossref.org/works/10.1076%2FAPAB.110.3.186.8294

retrieved

21 January 2018

Molecular and clinical aspects of mitochondrial diabetes mellitus

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https://api.crossref.org/works/10.1076%2FAPAB.110.3.186.8294

retrieved

21 January 2018

Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.

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reference URL

https://api.crossref.org/works/10.1076%2FAPAB.110.3.186.8294

retrieved

21 January 2018

Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria

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reference URL

https://api.crossref.org/works/10.1076%2FAPAB.110.3.186.8294

retrieved

21 January 2018

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

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reference URL

https://api.crossref.org/works/10.1076%2FAPAB.110.3.186.8294

retrieved

21 January 2018

Heteroplasmy levels of a mitochondrial gene mutation associated with diabetes mellitus decrease in leucocyte DNA upon aging

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reference URL

https://api.crossref.org/works/10.1076%2FAPAB.110.3.186.8294

retrieved

21 January 2018

Identifiers

DOI

10.1076/APAB.110.3.186.8294

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PubMed ID

12221518

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(Q57420556)

A Case of a De Novo A3243G Mutation in Mitochondrial DNA in a Patient with Diabetes and Deafness

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