(Q67543714)

English

Fatal cytochrome c oxidase-deficient myopathy of infancy associated with mtDNA depletion. Differential involvement of skeletal muscle and cultured fibroblasts

scientific article published on 01 January 1992

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1383604%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

Fatal cytochrome c oxidase-deficient myopathy of infancy associated with mtDNA depletion. Differential involvement of skeletal muscle and cultured fibroblasts (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1383604%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

author name string

N Telerman-Toppet

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1383604%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

D Biarent

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1383604%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

J M Bouton

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1383604%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

L de Meirleir

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1383604%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

C Elmer

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1383604%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

S Noel

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1383604%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

E Vamos

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1383604%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

S DiMauro

8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1383604%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

publication date

1 January 1992

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1383604%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

Journal of Inherited Metabolic Disease

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1383604%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

15

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1383604%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1383604%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

323-326

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1383604%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

https://scigraph.springernature.com/pub.10.1007/bf02435967

0 references

Differential diagnosis of fatal and benign cytochrome c oxidase-deficient myopathies of infancy: an immunohistochemical approach

1 reference

https://pubmed.ncbi.nlm.nih.gov/1383604

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/1383604

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytochrome c oxidase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/1383604

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region

1 reference

https://pubmed.ncbi.nlm.nih.gov/1383604

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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