(Q43510265)

24 November 2017

Identification of point mutations by mispairing PCR as exemplified in MERRF disease (English)

1 reference

24 November 2017

Seibel P

1

1 reference

24 November 2017

Degoul F

2

1 reference

24 November 2017

Romero N

3

1 reference

24 November 2017

Marsac C

4

1 reference

24 November 2017

Kadenbach B

5

1 reference

24 November 2017

language of work or name

English

0 references

publication date

1 December 1990

1 reference

Biochemical and Biophysical Research Communications

24 November 2017

1 reference

24 November 2017

173

1 reference

24 November 2017

2

1 reference

24 November 2017

561-565

1 reference

Familial mitochondrial encephalomyopathy (MERRF): genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease

24 November 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980071-3

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980071-3

DNA typing from single hairs

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980071-3

Sequence and organization of the human mitochondrial genome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980071-3

Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2980071-3

10.1016/S0006-291X(05)80071-3

7 January 2021

Identifiers

DOI

1 reference

24 November 2017

1 reference