(Q50518875)

English

Macular pattern dystrophy associated with a mutation of mitochondrial DNA.

scientific article published in August 1995

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/7639309

Macular pattern dystrophy associated with a mutation of mitochondrial DNA. (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/7639309

mitochondrial DNA

0 references

7

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/7639309

author name string

P Massin

1

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/7639309

P J Guillausseau

2

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/7639309

B Vialettes

3

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/7639309

V Paquis

4

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/7639309

F Orsini

5

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/7639309

A D Grimaldi

6

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/7639309

language of work or name

0 references

publication date

1 August 1995

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/7639309

American Journal of Ophthalmology

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/7639309

120

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/7639309

2

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/7639309

247-248

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/7639309

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972615-7

7 January 2021

Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972615-7

7 January 2021

The retinal manifestations of mitochondrial myopathy. A study of 22 cases

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972615-7

7 January 2021

Identifiers

10.1016/S0002-9394(14)72615-7

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/7639309

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/7639309

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