(Q71943526)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8982948%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

title

Complementation analysis of systemic cytochrome oxidase deficiency presenting as Leigh syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8982948%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

author name string

R M Brown

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8982948%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

G K Brown

series ordinal

2

1 reference

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22 October 2019

publication date

1 January 1996

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8982948%20AND%20SRC:MED&resulttype=core&format=json

Journal of Inherited Metabolic Disease

22 October 2019

published in

1 reference

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22 October 2019

volume

19

1 reference

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22 October 2019

issue

6

1 reference

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22 October 2019

page(s)

752-760

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf01799168

22 October 2019

exact match

0 references

cites work

Nuclear DNA origin of cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence based on patient's-derived rho degrees transformants

1 reference

12 December 2020

1 reference

12 December 2020

Heteroplasmic mtDNA mutation (T----G) at 8993 can cause Leigh disease when the percentage of abnormal mtDNA is high

1 reference

12 December 2020

Biochemical and molecular analysis of cytochrome c oxidase deficiency in Leigh's syndrome

1 reference

12 December 2020

Cytochrome c oxidase deficiency in subacute necrotizing encephalomyelopathy

1 reference

12 December 2020

Biochemical study in 28 children with lactic acidosis, in relation to Leigh's encephalomyelopathy

1 reference

12 December 2020

Cytochrome c oxidase deficiency in Leigh syndrome

1 reference

12 December 2020

Cytochrome c oxidase-associated Leigh syndrome: Phenotypic features and pathogenetic speculations

1 reference

12 December 2020

Characterization of cytochrome-c oxidase mutants in human fibroblasts

1 reference

12 December 2020

Cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence for a nuclear DNA-encoded mutation.

1 reference

12 December 2020

Nondroplet ultrastructural demonstration of cytochrome oxidase activity with a polymerizing osmiophilic reagent, diaminobenzidine (DAB).

1 reference

12 December 2020

Cytochrome c oxidase deficiency in subacute necrotizing encephalopathy (Leigh syndrome)

1 reference

12 December 2020

Molecular genetic characterization of an X-linked form of Leigh's syndrome

1 reference

12 December 2020

Immunochemical study in three patients with cytochrome c oxidase deficiency presenting Leigh's encephalomyelopathy

1 reference

12 December 2020

Cytochrome c oxidase deficiency in three patients with Leigh's disease

1 reference

12 December 2020

Subacute necrotizing encephalomyelopathy in an infant

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01799168

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8982948%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

1 reference