Citations for
1EOD, PRNP
Inherited prion disease with 5-OPRI: phenotype modification by repeat length and codon 129.
Mead S, Webb TE, Campbell TA, Beck J, Linehan JM, Rutherfoord S, Joiner S, Wadsworth JD, Heckmann J, Wroe S, Doey L, King A, Collinge J.
Neurology 69(8):730-8. 2007
2EOD, PRNP
Inherited prion encephalopathy associated with the novel PRNP H187R mutation: a clinical study.
Butefisch CM, Gambetti P, Cervenakova L, Park KY, Hallett M, Goldfarb LG.
Neurology 55(4):517-22. 2000