(Q50455813)

English

Prevalence, segregation, and phenotype of the mitochondrial DNA 3243A>G mutation in children.

scientific article published in September 2007

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17823937

Prevalence, segregation, and phenotype of the mitochondrial DNA 3243A>G mutation in children. (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17823937

mitochondrial DNA

0 references

Jukka S Moilanen

object named as

Jukka S Moilanen

2

0 references

Elina Mäki-Torkko

8

object named as

Elina Mäki-Torkko

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17823937

author name string

Johanna Uusimaa

1

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17823937

Leena Vainionpää

3

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17823937

Päivi Tapanainen

4

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17823937

Päivi Lindholm

5

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17823937

Matti Nuutinen

6

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17823937

Tuija Löppönen

7

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17823937

Heikki Rantala

9

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17823937

Kari Majamaa

10

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17823937

publication date

1 September 2007

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17823937

Annals of Neurology

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17823937

62

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17823937

3

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17823937

278-287

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17823937

Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotype.

1 reference

https://api.crossref.org/works/10.1002%2FANA.21196

21 January 2018

Epileptic phenotypes associated with mitochondrial disorders.

1 reference

https://api.crossref.org/works/10.1002%2FANA.21196

21 January 2018

Nonsyndromic hearing loss: an analysis of audiograms.

1 reference

https://api.crossref.org/works/10.1002%2FANA.21196

21 January 2018

Transmission of the human mitochondrial genome

1 reference

https://api.crossref.org/works/10.1002%2FANA.21196

21 January 2018

Mitochondrial genotype segregation and the bottleneck

1 reference

https://api.crossref.org/works/10.1002%2FANA.21196

21 January 2018

Identifiers

10.1002/ANA.21196

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17823937

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/17823937

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