(Q48649113)

English

Maternally inherited encephalopathy associated with a single-base insertion in the mitochondrial tRNATrp gene.

scientific article published in August 1997

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scholarly article

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9266739

Maternally inherited encephalopathy associated with a single-base insertion in the mitochondrial tRNATrp gene. (English)

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9266739

author name string

Santorelli FM

1

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9266739

Tanji K

2

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9266739

Sano M

3

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9266739

Shanske S

4

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9266739

El-Shahawi M

5

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9266739

Kranz-Eble P

6

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9266739

DiMauro S

7

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9266739

De Vivo DC

8

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9266739

publication date

1 August 1997

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9266739

Annals of Neurology

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9266739

42

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9266739

256-260

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9266739

2

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9266739

Complementation of mutant and wild-type human mitochondrial DNAs coexisting since the mutation event and lack of complementation of DNAs introduced separately into a cell within distinct organelles

1 reference

https://api.crossref.org/works/10.1002%2FANA.410420220

21 January 2018

Identifiers

10.1002/ANA.410420220

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9266739

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/9266739

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