(Q71872901)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7609445%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

title

Enzymological versus DNA investigations in mitochondrial (encephalo-) myopathies (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7609445%20AND%20SRC:MED&resulttype=core&format=json

https://api.crossref.org/works/10.1007/BF00711674

21 October 2019

Enzymological versus DNA investigations in mitochondrial (encephalo‐)myopathies (English)

1 reference

15 June 2024

author name string

D. D. de Vries

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7609445

15 June 2024

W. Ruitenbeek

2

1 reference

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15 June 2024

I. J. de Wijs

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7609445

15 June 2024

J. M. Trijbels

4

1 reference

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15 June 2024

B. A. van Oost

5

1 reference

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15 June 2024

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7609445

15 June 2024

publication date

1 January 1993

1 reference

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full work available at URL

21 October 2019

https://onlinelibrary.wiley.com/doi/pdf/10.1007/BF00711674

1 reference

https://api.crossref.org/works/10.1007/BF00711674

Journal of Inherited Metabolic Disease

15 June 2024

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7609445%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

volume

16

1 reference

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21 October 2019

issue

3

1 reference

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21 October 2019

page(s)

534-536

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf00711674

21 October 2019

exact match

0 references

cites work

Defects of mitochondrial DNA

1 reference

12 December 2020

Mitochondrial mutation in fatal infantile cardiomyopathy

1 reference

12 December 2020

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

1 reference

12 December 2020

A mitochondrial encephalomyopathy: the first case with an established defect at the level of coenzyme Q.

1 reference

12 December 2020

Myopathology and a mitochondrial DNA deletion in the Pearson marrow and pancreas syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Disorders of the mitochondrial respiratory chain: clinical manifestations and diagnostic approach

1 reference

12 December 2020

Biogenesis of mitochondria

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00711674

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7609445%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

1 reference