(Q28511239)

25 January 2017

title

Primary biochemical defect in copper metabolism in mice with a recessive X-linked mutation analogous to Menkes' disease in man (English)

1 reference

ATPase, Cu++ transporting, alpha polypeptide

25 January 2017

main subject

1 reference

GOA release 2020-03-11

1 reference

https://api.crossref.org/works/10.1016/S0162-0134(00)81002-8

20 July 2023

1 reference

https://api.crossref.org/works/10.1016/S0162-0134(00)81002-8

20 July 2023

author name string

H. W. Prins

series ordinal

1

1 reference

25 January 2017

C. J. Van den Hamer

series ordinal

2

1 reference

25 January 2017

language of work or name

1 reference

1 February 1979

1 reference

full work available at URL

25 January 2017

https://api.elsevier.com/content/article/PII:S0162013400810028?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/S0162-0134(00)81002-8

https://api.elsevier.com/content/article/PII:S0162013400810028?httpAccept=text/plain

20 July 2023

1 reference

https://api.crossref.org/works/10.1016/S0162-0134(00)81002-8

Journal of Inorganic Biochemistry

20 July 2023

published in

1 reference

25 January 2017

volume

10

1 reference

25 January 2017

issue

1

1 reference

25 January 2017

page(s)

19–27

1 reference

Primary defect in copper transport underlies mottled mutants in the mouse

25 January 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0162-0134%2800%2981002-8

inferred from DOI database lookup

7 January 2021

based on heuristic

Comparative biochemistry and physiology

3

57c

79

Hunt

1977

1 reference

https://api.crossref.org/works/10.1016/S0162-0134(00)81002-8

20 July 2023

Identifiers

0 references

1 reference