Familial myopathy: new insights into the T14709C mitochondrial tRNA mutation. (Q44817599)

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26 December 2019

title

Familial myopathy: new insights into the T14709C mitochondrial tRNA mutation (English)

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26 December 2019

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26 December 2019

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26 December 2019

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26 December 2019

Patrick F Chinnery

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26 December 2019

Robert William Taylor

object named as

Robert W Taylor

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Douglass Matthew Turnbull

26 December 2019

object named as

Douglass M Turnbull

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26 December 2019

Julie L Gardner

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26 December 2019

Stephen Lynn

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26 December 2019

Christine M Hayes

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26 December 2019

Mark Walker

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26 December 2019

publication date

1 April 2004

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26 December 2019

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26 December 2019

volume

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26 December 2019

issue

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26 December 2019

page(s)

478-484

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Early onset of diabetes mellitus associated with the mitochondrial DNA T14709C point mutation: patient report and literature review

26 December 2019

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FANA.20004

Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA(Ser(UCN)) gene

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FANA.20004

Molecular and functional effects of the T14709C point mutation in the mitochondrial DNA of a patient with maternally inherited diabetes and deafness

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FANA.20004

21 January 2018

Identifiers

DOI

10.1002/ANA.20004

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26 December 2019

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