(Q50429690)

13 March 2018

title

Mitochondrial DNA haplogroup associated with hereditary hearing loss in a Japanese population. (English)

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13 March 2018

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5

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author name string

Tomofumi Kato

1

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Noriyuki Fuku

2

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Yoshihiro Noguchi

3

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Haruka Murakami

4

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Yurika Kimura

6

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Masashi Tanaka

7

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Ken Kitamura

8

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language of work or name

English

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publication date

25 July 2012

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13 March 2018

published in

Acta Oto-Laryngologica

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volume

132

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issue

11

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page(s)

1178-1182

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Newborn hearing screening--a silent revolution

cites work

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https://api.crossref.org/works/10.3109%2F00016489.2012.693624

21 January 2018

Mitochondrial disease

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https://api.crossref.org/works/10.3109%2F00016489.2012.693624

Hearing impairment risk and interaction of folate metabolism related gene polymorphisms in an aging study

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Association of interleukin-1 gene polymorphisms with sudden sensorineural hearing loss and Ménière's disease.

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https://api.crossref.org/works/10.3109%2F00016489.2012.693624

Vertebrobasilar occlusive disorders presenting as sudden sensorineural hearing loss.

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https://api.crossref.org/works/10.3109%2F00016489.2012.693624

Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss

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https://api.crossref.org/works/10.3109%2F00016489.2012.693624

Mitochondrial genome variation in eastern Asia and the peopling of Japan

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https://api.crossref.org/works/10.3109%2F00016489.2012.693624

Applications of Luminex xMAP technology for rapid, high-throughput multiplexed nucleic acid detection

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https://api.crossref.org/works/10.3109%2F00016489.2012.693624

Mitochondrial haplogroup N9a confers resistance against type 2 diabetes in Asians

21 January 2018

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https://api.crossref.org/works/10.3109%2F00016489.2012.693624

Phylogeographic differentiation of mitochondrial DNA in Han Chinese

21 January 2018

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https://api.crossref.org/works/10.3109%2F00016489.2012.693624

Mitochondrial 12S rRNA gene mutations affect RNA secondary structure and lead to variable penetrance in hearing impairment

21 January 2018

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https://api.crossref.org/works/10.3109%2F00016489.2012.693624

Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss

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https://api.crossref.org/works/10.3109%2F00016489.2012.693624

Mitochondrial ND5 T12338C, tRNA(Cys) T5802C, and tRNA(Thr) G15927A variants may have a modifying role in the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese pedigrees.

21 January 2018

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https://api.crossref.org/works/10.3109%2F00016489.2012.693624

Polymorphisms in control region of mtDNA relates to individual differences in endurance capacity or trainability.

21 January 2018

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https://api.crossref.org/works/10.3109%2F00016489.2012.693624

Endothelin-1 gene polymorphism and hearing impairment in elderly Japanese

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F00016489.2012.693624

PCA and clustering reveal alternate mtDNA phylogeny of N and M clades

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https://api.crossref.org/works/10.3109%2F00016489.2012.693624

Audiologic findings in patients with a point mutation at nucleotide 3,243 of mitochondrial DNA.

21 January 2018

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https://api.crossref.org/works/10.3109%2F00016489.2012.693624

10.3109/00016489.2012.693624

21 January 2018

Identifiers

DOI

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13 March 2018

PubMed ID

22830575

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13 March 2018