Methionine homozygosity at prion gene codon 129 may predispose to sporadic inclusion-body myositis
Lancet
.
1999 Feb 6;353(9151):465-6.
doi: 10.1016/S0140-6736(98)05208-8.
Authors
J Lampe
,
H Kitzler
,
M C Walter
,
H Lochmüller
,
H Reichmann
PMID:
9989722
DOI:
10.1016/S0140-6736(98)05208-8
No abstract available
Publication types
Letter
MeSH terms
Codon / genetics*
Genetic Predisposition to Disease*
Homozygote
Humans
Methionine / genetics*
Middle Aged
Myositis, Inclusion Body / genetics*
Prions / genetics*
Substances
Codon
Prions
Methionine