(Q49197990)

English

High mitochondrial DNA T8993G mutation (<90%) without typical features of Leigh's and NARP syndromes.

scientific article published in July 2001

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

19 February 2018

http://europepmc.org/abstract/MED/11453454

High mitochondrial DNA T8993G mutation (<90%) without typical features of Leigh's and NARP syndromes. (English)

1 reference

Europe PubMed Central

PubMed publication ID

19 February 2018

http://europepmc.org/abstract/MED/11453454

mitochondrial DNA

0 references

author name string

C Y Tsao

1

1 reference

Europe PubMed Central

PubMed publication ID

19 February 2018

http://europepmc.org/abstract/MED/11453454

J R Mendell

2

1 reference

Europe PubMed Central

PubMed publication ID

19 February 2018

http://europepmc.org/abstract/MED/11453454

D Bartholomew

3

1 reference

Europe PubMed Central

PubMed publication ID

19 February 2018

http://europepmc.org/abstract/MED/11453454

publication date

1 July 2001

1 reference

Europe PubMed Central

PubMed publication ID

19 February 2018

http://europepmc.org/abstract/MED/11453454

Journal of Child Neurology

1 reference

Europe PubMed Central

PubMed publication ID

19 February 2018

http://europepmc.org/abstract/MED/11453454

16

1 reference

Europe PubMed Central

PubMed publication ID

19 February 2018

http://europepmc.org/abstract/MED/11453454

7

1 reference

Europe PubMed Central

PubMed publication ID

19 February 2018

http://europepmc.org/abstract/MED/11453454

533-535

1 reference

Europe PubMed Central

PubMed publication ID

19 February 2018

http://europepmc.org/abstract/MED/11453454

Mitochondrial DNA 8993 (NARP) mutation presenting with a heterogeneous phenotype including 'cerebral palsy'.

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600716

21 January 2018

Maternally inherited Leigh syndrome.

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600716

21 January 2018

Mitochondrial DNA mutation and Leigh's syndrome

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600716

21 January 2018

Suppression of a mitochondrial tRNA gene mutation phenotype associated with changes in the nuclear background

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600716

21 January 2018

Identifiers

10.1177/088307380101600716

1 reference

Europe PubMed Central

PubMed publication ID

19 February 2018

http://europepmc.org/abstract/MED/11453454

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 February 2018

http://europepmc.org/abstract/MED/11453454

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