Influence of homozygosity for methionine at codon 129 of the human prion gene on the onset of neurological and hepatic symptoms in Wilson disease.

Merle, Uta

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] - Archives of neurology Jul 2006 - 982-5 p. digital

Publication Type: Journal Article

0003-9942

10.1001/archneur.63.7.982 doi


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