(Q43967268)

28 November 2017

Mitochondrial encephalopathies: molecular genetic diagnosis from blood samples (English)

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)92981-7

26 October 2022

2

M. G. Sweeney

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1674297

26 October 2022

John A. Morgan-Hughes

4

object named as

J. A. Morgan-Hughes

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1674297

26 October 2022

author name string

S. R. Hammans

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1674297

26 October 2022

M. Brockington

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1674297

26 October 2022

A. E. Harding

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1674297

26 October 2022

language of work or name

English

0 references

publication date

1 June 1991

1 reference

full work available at URL

28 November 2017

https://api.elsevier.com/content/article/PII:0140673691929817?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)92981-7

https://api.elsevier.com/content/article/PII:0140673691929817?httpAccept=text/plain

26 October 2022

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)92981-7

26 October 2022

1 reference

28 November 2017

337

1 reference

28 November 2017

1311-1313

1 reference

28 November 2017

8753

1 reference

Mitochondrial myopathies: clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA

28 November 2017

1

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)92981-7

Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome.

26 October 2022

2

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)92981-7

Duplications of mitochondrial DNA in mitochondrial myopathy

26 October 2022

3

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)92981-7

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

26 October 2022

4

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)92981-7

A new mitochondrial disease associated with mitochondrial DNA heteroplasmy

26 October 2022

5

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)92981-7

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

26 October 2022

6

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)92981-7

Myoclonus epilepsy and ragged-red fibres (MERRF). 1. A clinical, pathological, biochemical, magnetic resonance spectrographic and positron emission tomographic study

26 October 2022

7

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)92981-7

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.

26 October 2022

8

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)92981-7

Classification of progressive myoclonus epilepsies and related disorders

26 October 2022

9

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)92981-7

Sequence and organization of the human mitochondrial genome

26 October 2022

11

1 reference

https://api.crossref.org/works/10.1016/0140-6736(91)92981-7

26 October 2022

Identifiers

1 reference

28 November 2017

1 reference