Human lysyl oxidase and hereditary diseases of copper metabolism : structure of the human lysyl oxidase gene, its expression in malignant cells and cells from patients with Menkes disease, and characterization of mutations in the Wilson disease gene

Human lysyl oxidase and hereditary diseases of copper metabolism : structure of the human lysyl oxidase gene, its expression in malignant cells and cells from patients with Menkes disease, and characterization of mutations in the Wilson disease gene

datePublished

• 1996

description

• kuvitettu
• Tiivistelmä ja 4 erip.

identifier

• propertyID: FI-FENNI value: 533618
• propertyID: FI-MELINDA value: 003242178
• propertyID: skl value: fx533618

isbn

• 9514244680

isPartOf

• Acta universitatis Ouluensis, Electronica
• Fennica

name

• Human lysyl oxidase and hereditary diseases of copper metabolism : structure of the human lysyl oxidase gene, its expression in malignant cells and cells from patients with Menkes disease, and characterization of mutations in the Wilson disease gene

numberOfPages

• 56, [21] s.

P60048

• <http://rdaregistry.info/termList/RDACarrierType/1049>

P60050

• <http://rdaregistry.info/termList/RDAMediaType/1007>

publication

• location: Oulu organizer: Oulun yliopisto

publisher

• Oulun yliopisto