NR ACLK
AU Cervenakova,L.; Sivakumar,K.; Nagle,J.; Dalakas,M.C.; Goldfarb,L.G.
TI Is hereditary inclusion body myopathy a "familial prion disease" ?
QU Annals of Neurology 1996 Jul; 40(1): 128
PT letter
MH Chromosomes, Human, Pair 20; Human; *Inclusion Bodies; Prion Diseases/*genetics
SP englisch
PO USA