Influence of homozygosity for methionine at codon 129 of the human prion gene on the onset of neurological and hepatic symptoms in Wilson disease. [electronic resource]
Producer: 20060807Description: 982-5 p. digitalISSN:- 0003-9942
- Adolescent
- Adult
- Age of Onset
- Apolipoprotein E3
- Apolipoproteins E -- genetics
- Codon
- Copper -- metabolism
- Cross-Sectional Studies
- Female
- Genotype
- Hepatolenticular Degeneration -- complications
- Homozygote
- Humans
- Liver Diseases -- etiology
- Male
- Methionine -- genetics
- Nervous System Diseases -- etiology
- Polymorphism, Genetic
- Prions -- genetics
- Retrospective Studies
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Publication Type: Journal Article
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