NR AGZF

AU Lampe,J.; Kitzler,H.; Walter,M.C.; Lochmüller,H.; Reichmann,H.

TI Methionine homozygosity at prion gene codon 129 may predispose to sporadic inclusion-body myositis

QU Lancet 1999 Feb 6; 353(9151): 465-6

PT letter

MH Codon/*genetics; *Genetic Predisposition to Disease; Homozygote; Human; Methionine/*genetics; Middle Age; Myositis, Inclusion Body/*genetics; Prions/*genetics

SP englisch

PO England

EA pdf-Datei

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