Sporadic inclusion body myositis not linked to prion protein codon 129 methionine homozygosity
Neurology
.
2000 Oct 24;55(8):1235.
doi: 10.1212/wnl.55.8.1235.
Authors
M Orth
1
,
S J Tabrizi
,
A H Schapira
Affiliation
1
University Department of Clinical Neurosciences, Royal Free and University College Medical School, London, UK.
PMID:
11071511
DOI:
10.1212/wnl.55.8.1235
No abstract available
MeSH terms
Genetic Linkage / genetics*
Homozygote
Humans
Methionine / genetics*
Middle Aged
Myositis, Inclusion Body / genetics*
Prions / genetics*
Substances
Prions
Methionine