(Q41283179)

29 September 2017

1 reference

title

Mitochondrial genetics and human disease (English)

1 reference

29 September 2017

Grossman LI

1

1 reference

PubMed ID

8976155

29 September 2017

Shoubridge EA

series ordinal

2

1 reference

PubMed ID

8976155

29 September 2017

language of work or name

English

0 references

publication date

1 December 1996

1 reference

29 September 2017

1 reference

29 September 2017

18

1 reference

29 September 2017

983-991

1 reference

29 September 2017

12

1 reference

Transcriptional activation through ETS domain binding sites in the cytochrome c oxidase subunit IV gene

29 September 2017

1 reference

https://api.crossref.org/works/10.1002%2FBIES.950181208

Widespread tissue distribution of mitochondrial DNA deletions in Kearns-Sayre syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBIES.950181208

Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBIES.950181208

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBIES.950181208

Dominantly inherited mitochondrial myopathy with multiple deletions of mitochondrial DNA: clinical, morphologic, and biochemical studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FBIES.950181208

21 January 2018

Identifiers

DOI

10.1002/BIES.950181208

1 reference

29 September 2017

1 reference

PubMed ID

8976155