Related Experiment Videos

The effects of heredity and environment on copper metabolism

The Medical Clinics of North America

|July 1, 1976

Abstract

No abstract available in PubMed .

Related Concept Videos

Articles linked to this work by shared authors, journal, and citation graph.

Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation.

Human molecular genetics·1999

Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses.

American journal of human genetics·1997

Wilson disease and idiopathic copper toxicosis.

The American journal of clinical nutrition·1996

Rate of information processing in patients with Wilson's disease.

The Journal of neuropsychiatry and clinical neurosciences·1995

Is non-Indian childhood cirrhosis caused by excess dietary copper?

Lancet (London, England)·1994

Liver transplantation for Wilson's disease: indications and outcome.

Hepatology (Baltimore, Md.)·1994

See all related articles