(Q50509400)

English

Familial clustering strongly suggests that the phenotypic variation of the 8344 A>G lys mitochondrial tRNA mutation is encoded in cis.

scientific article published in July 2012

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/22681518

Familial clustering strongly suggests that the phenotypic variation of the 8344 A>G lys mitochondrial tRNA mutation is encoded in cis. (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/22681518

Constantin Polychronakos

7

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/22681518

author name string

Kyriakos Kazakos

1

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/22681518

Kalliopi Kotsa

2

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/22681518

Maria Yavropoulou

3

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/22681518

Alexander Dionyssopoulos

4

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/22681518

Rosemary Grabs

5

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/22681518

John Yovos

6

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/22681518

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publication date

1 July 2012

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/22681518

Annals of Human Genetics

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Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/22681518

76

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/22681518

4

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/22681518

296-300

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/22681518

Current classification of mitochondrial disorders

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2012.00711.X

21 January 2018

Expanding the phenotype of the 8344 transfer RNAlysine mitochondrial DNA mutation.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2012.00711.X

21 January 2018

Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2012.00711.X

21 January 2018

The mitochondrial DNA genetic bottleneck results from replication of a subpopulation of genomes

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2012.00711.X

21 January 2018

Nuclear genetic control of mitochondrial DNA segregation

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2012.00711.X

21 January 2018

Identifiers

10.1111/J.1469-1809.2012.00711.X

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/22681518

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/22681518

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