(Q39509017)

12 September 2017

1 reference

title

Cytochrome oxidase deficiency: clinical and biochemical heterogeneity (English)

1 reference

12 September 2017

DiMauro S

1

1 reference

12 September 2017

Zeviani M

2

1 reference

12 September 2017

Servidei S

3

1 reference

12 September 2017

Bonilla E

4

1 reference

12 September 2017

Miranda AF

5

1 reference

12 September 2017

Prelle A

6

1 reference

12 September 2017

Schon EA

7

1 reference

12 September 2017

language of work or name

English

0 references

publication date

1 January 1986

1 reference

Annals of the New York Academy of Sciences

12 September 2017

number of pages

14

1 reference

based on heuristic

inferred from page(s)

published in

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12 September 2017

volume

488

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12 September 2017

page(s)

19-32

1 reference

Isolation and properties of cytochrome c oxidase from rat liver and quantification of immunological differences between isozymes from various rat tissues with subunit-specific antisera

12 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1986.TB46545.X

Structure of cytochrome c oxidase

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1986.TB46545.X

Fatal infantile cytochrome c oxidase deficiency: decrease of immunologically detectable enzyme in muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1986.TB46545.X

Mitochondrial cytochrome deficiency presenting as a myopathy with hypotonia, external ophthalmoplegia, and lactic acidosis in an infant and as fatal hepatopathy in a second cousin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1986.TB46545.X

Two siblings with cytochromec oxidase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1986.TB46545.X

Progressive poliodystrophy (Alpers' disease) with a defect in cytochrome aa3 in muscle: a report of two unrelated patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1986.TB46545.X

Trichopoliodystrophy. I. Report of a case and biochemical studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1986.TB46545.X

A partial deficiency of cytochrome c oxidase in chronic progressive external ophthalmoplegia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1986.TB46545.X

Maternal inheritance of human mitochondrial DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1986.TB46545.X

Sequence and organization of the human mitochondrial genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1986.TB46545.X

Mitochondrial inheritance and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1986.TB46545.X

10.1111/J.1749-6632.1986.TB46545.X

21 January 2018

Identifiers

DOI

1 reference

12 September 2017

1 reference