TY  - GEN
AU  - Merle,Uta
AU  - Stremmel,Wolfgang
AU  - Gessner,Reinhard
TI  - Influence of homozygosity for methionine at codon 129 of the human prion gene on the onset of neurological and hepatic symptoms in Wilson disease
SN  - 0003-9942
PY  - 2006///0807
KW  - Adolescent
KW  - Adult
KW  - Age of Onset
KW  - Apolipoprotein E3
KW  - Apolipoproteins E
KW  - genetics
KW  - Codon
KW  - Copper
KW  - metabolism
KW  - Cross-Sectional Studies
KW  - Female
KW  - Genotype
KW  - Hepatolenticular Degeneration
KW  - complications
KW  - Homozygote
KW  - Humans
KW  - Liver Diseases
KW  - etiology
KW  - Male
KW  - Methionine
KW  - Nervous System Diseases
KW  - Polymorphism, Genetic
KW  - Prions
KW  - Retrospective Studies
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1001/archneur.63.7.982
ER  -