(Q40559254)

21 September 2017

title

Molecular pathogenetic mechanism of maternally inherited deafness (English)

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21 September 2017

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Min-Xin Guan

1

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21 September 2017

language of work or name

English

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publication date

1 April 2004

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Annals of the New York Academy of Sciences

21 September 2017

published in

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21 September 2017

volume

1011

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21 September 2017

page(s)

259-271

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Deletions of mitochondrial DNA in Kearns-Sayre syndrome. 1988.

21 September 2017

cites work

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https://api.crossref.org/works/10.1196%2FANNALS.1293.025

A new mtDNA mutation associated with a progressive encephalopathy and cytochrome c oxidase deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1293.025

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

https://api.crossref.org/works/10.1196%2FANNALS.1293.025

The deafness-associated mitochondrial DNA mutation at position 7445, which affects tRNASer(UCN) precursor processing, has long-range effects on NADH dehydrogenase subunit ND6 gene expression.

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1293.025

Aminoglycoside-induced hearing loss in a patient with the 961 mutation in mitochondrial DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1293.025

21 January 2018

Identifiers

DOI

10.1196/ANNALS.1293.025

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21 September 2017

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