(Q38485824)

3 September 2017

Sequencing and quantitative assessment of mutant and wild-type mitochondrial DNA in paraffin sections from cases of MELAS. (English)

1 reference

3 September 2017

0 references

Love S

1

1 reference

PubMed ID

8326463

3 September 2017

Nicoll JA

series ordinal

2

1 reference

PubMed ID

8326463

3 September 2017

Kinrade E

series ordinal

3

1 reference

3 September 2017

1 May 1993

1 reference

3 September 2017

1 reference

3 September 2017

170

1 reference

3 September 2017

1

1 reference

3 September 2017

9-14

1 reference

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutation

3 September 2017

1 reference

https://api.crossref.org/works/10.1002%2FPATH.1711700103

Crossref

reference URL

Widespread tissue distribution of a tRNALeu(UUR) mutation in the mitochondrial DNA of a patient with MELAS syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPATH.1711700103

Crossref

reference URL

A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FPATH.1711700103

Crossref

reference URL

21 January 2018

Identifiers

DOI

10.1002/PATH.1711700103

1 reference

3 September 2017

1 reference

PubMed ID

8326463