Cytochrome oxidase deficiency in Wilson's disease: a suggested ceruloplasmin function.

about

Genome-wide analysis of human disease alleles reveals that their locations are correlated in paralogous proteins.A genetic study of Wilson's disease: evidence for heterogeneity.The role of ceruloplasmin in iron metabolism.Ceruloplasmin: methods and clinical use.

P2860

Q33383215-603739B5-D8C9-458E-B12F-8FDB7C8565CC Q35569385-5BCC45E3-EAE7-4C78-81A9-E6E66652EE75 Q35582301-57DD510E-4279-48D3-A3ED-10D3777542F3 Q40244681-FA926617-0333-44FC-AFFB-7E12B1085565

P2860

Cytochrome oxidase deficiency in Wilson's disease: a suggested ceruloplasmin function.

Item

http://www.wikidata.org/entity/Q36450857

description

1969 nî lūn-bûn

@nan

1969年の論文

@ja

1969年学术文章

@wuu

1969年学术文章

@zh-cn

1969年学术文章

@zh-hans

1969年学术文章

@zh-my

1969年学术文章

@zh-sg

1969年學術文章

@yue

1969年學術文章

@zh

1969年學術文章

@zh-hant

name

Cytochrome oxidase deficiency in Wilson's disease: a suggested ceruloplasmin function.

@ast

Cytochrome oxidase deficiency in Wilson's disease: a suggested ceruloplasmin function.

@en

type

Item

label

Cytochrome oxidase deficiency in Wilson's disease: a suggested ceruloplasmin function.

@ast

Cytochrome oxidase deficiency in Wilson's disease: a suggested ceruloplasmin function.

@en

prefLabel

Cytochrome oxidase deficiency in Wilson's disease: a suggested ceruloplasmin function.

@ast

Cytochrome oxidase deficiency in Wilson's disease: a suggested ceruloplasmin function.

@en

P1476

Cytochrome oxidase deficiency in Wilson's disease: a suggested ceruloplasmin function.

@en

P2093

Shokeir MH

http://www.w3.org/2001/XMLSchema#string

Shreffler DC

http://www.w3.org/2001/XMLSchema#string

P2860

The amino acid content of the blood and urine in Wilson's disease.

Studies on copper metabolism. XIII. Hepatolenticular degeneration

Renal function in Wilson's disease.

Exchange of ceruloplasmin copper with ionic Cu64 with reference to Wilson's disease.

Deficiency of ceruloplasmin in patients with hepatolenticular degeneration (Wilson's disease).

Leukocyte oxidase: defective activity in chronic granulomatous disease.

Chromosome preparations of leukocytes cultured from human peripheral blood.

INVESTIGATION OF THE AMINOACIDURIA IN WILSON'S DISEASE (HEPATOLENTICULAR DEGENERATION): DEMONSTRATION OF A DEFECT IN RENAL FUNCTION.

Abnormalities of copper metabolism in Wilson's disease and their relationship to the aminoaciduria.

Oral contraceptives and caeruloplasmin activity.

P304

867-872

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1073/PNAS.62.3.867

http://www.w3.org/2001/XMLSchema#string

P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

1969-03-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

18857961

http://www.w3.org/2001/XMLSchema#string

P698

4308098

http://www.w3.org/2001/XMLSchema#string

P932

223678

http://www.w3.org/2001/XMLSchema#string

Cytochrome oxidase deficiency in Wilson's disease: a suggested ceruloplasmin function.

about

P2860

P2860

Cytochrome oxidase deficiency in Wilson's disease: a suggested ceruloplasmin function.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P5875

P698

P932