(Q50456640)

English

Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip.

scientific article published on 18 July 2007

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scholarly article

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Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17637808

Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip. (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17637808

mitochondrial DNA

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1 reference

based on heuristic

inferred from title

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based on heuristic

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Christine Petit

23

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Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17637808

Sylvain Baulande

object named as

Sylvain Baulande

7

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object named as

Pascal Reynier

5

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object named as

Didier Lacombe

9

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Vincent Procaccio

object named as

Vincent Procaccio

4

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Eréa-Noel Garabedian

22

object named as

Eréa-Noël Garabedian

1 reference

Europe PubMed Central

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14 March 2018

http://europepmc.org/abstract/MED/17637808

author name string

Marianne Lévêque

1

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Europe PubMed Central

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14 March 2018

http://europepmc.org/abstract/MED/17637808

Sandrine Marlin

2

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14 March 2018

http://europepmc.org/abstract/MED/17637808

Laurence Jonard

3

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Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17637808

Patrizia Amati-Bonneau

6

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14 March 2018

http://europepmc.org/abstract/MED/17637808

Denis Pierron

8

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14 March 2018

http://europepmc.org/abstract/MED/17637808

Françoise Duriez

10

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Europe PubMed Central

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14 March 2018

http://europepmc.org/abstract/MED/17637808

Christine Francannet

11

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Europe PubMed Central

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14 March 2018

http://europepmc.org/abstract/MED/17637808

Thierry Mom

12

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Europe PubMed Central

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14 March 2018

http://europepmc.org/abstract/MED/17637808

Hubert Journel

13

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Europe PubMed Central

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14 March 2018

http://europepmc.org/abstract/MED/17637808

Hélène Catros

14

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14 March 2018

http://europepmc.org/abstract/MED/17637808

Valérie Drouin-Garraud

15

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14 March 2018

http://europepmc.org/abstract/MED/17637808

Marie-Françoise Obstoy

16

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14 March 2018

http://europepmc.org/abstract/MED/17637808

Hélène Dollfus

17

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Europe PubMed Central

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14 March 2018

http://europepmc.org/abstract/MED/17637808

Marie-Madeleine Eliot

18

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Europe PubMed Central

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14 March 2018

http://europepmc.org/abstract/MED/17637808

Laurence Faivre

19

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14 March 2018

http://europepmc.org/abstract/MED/17637808

Christian Duvillard

20

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Europe PubMed Central

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14 March 2018

http://europepmc.org/abstract/MED/17637808

Remy Couderc

21

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Europe PubMed Central

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14 March 2018

http://europepmc.org/abstract/MED/17637808

Delphine Feldmann

24

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Europe PubMed Central

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14 March 2018

http://europepmc.org/abstract/MED/17637808

Françoise Denoyelle

25

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Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17637808

publication date

18 July 2007

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14 March 2018

http://europepmc.org/abstract/MED/17637808

European Journal of Human Genetics

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14 March 2018

http://europepmc.org/abstract/MED/17637808

15

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14 March 2018

http://europepmc.org/abstract/MED/17637808

11

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14 March 2018

http://europepmc.org/abstract/MED/17637808

1145-1155

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Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17637808

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201891

0 references

Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201891

21 January 2018

Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201891

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201891

21 January 2018

Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201891

21 January 2018

Phenotype of non-syndromic deafness associated with the mitochondrial A1555G mutation is modulated by mitochondrial RNA modifying enzymes MTO1 and GTPBP3

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201891

21 January 2018

Two large French pedigrees with non syndromic sensorineural deafness and the mitochondrial DNA T7511C mutation: evidence for a modulatory factor.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201891

21 January 2018

The Human MitoChip: a high-throughput sequencing microarray for mitochondrial mutation detection.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201891

21 January 2018

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201891

21 January 2018

Phylogenetic network for European mtDNA.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201891

21 January 2018

mtDB: Human Mitochondrial Genome Database, a resource for population genetics and medical sciences

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201891

21 January 2018

Mitochondrial genome single nucleotide polymorphisms and their phenotypes in the Japanese.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201891

21 January 2018

Mitochondrial genome variation in eastern Asia and the peopling of Japan

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201891

21 January 2018

An enhanced MITOMAP with a global mtDNA mutational phylogeny

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201891

21 January 2018

Rapidly progressive neurodegeneration in a case with the 7472insC mutation and the A7472C polymorphism in the mtDNA tRNA ser(UCN) gene

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201891

21 January 2018

Multiple origins of the mtDNA 7472insC mutation associated with hearing loss and neurological dysfunction.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201891

21 January 2018

A reappraisal of complete mtDNA variation in East Asian families with hearing impairment

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201891

21 January 2018

Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201891

21 January 2018

Sequence variation in mitochondrial complex I genes: mutation or polymorphism?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201891

21 January 2018

GUG is an efficient initiation codon to translate the human mitochondrial ATP6 gene

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201891

21 January 2018

An oligonucleotide microarray for high-throughput sequencing of the mitochondrial genome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201891

21 January 2018

Mitochondrial dysfunction in hearing loss.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201891

21 January 2018

Bilateral sensorineural hearing loss in members of a maternal lineage with mitochondrial point mutation.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201891

7 January 2021

based on heuristic

inferred from DOI database lookup

Extreme variability of clinical symptoms among sibs in a MELAS family correlated with heteroplasmy for the mitochondrial A3243G mutation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201891

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/SJ.EJHG.5201891

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17637808

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17637808

ResearchGate publication ID

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