A. Nieto

The molecular genetics of familial Creutzfeldt-Jakob disease in France

P. Brown, D. Gajdusek, L. Goldfarb, 1991, Journal of the Neurological Sciences.

Creutzfeldt‐Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European origin

P. Brown, D. Gajdusek, D. Asher, 1992, Annals of neurology.

Familial Creutzfeldt-Jakob disease in Chile is associated with the codon 200 mutation of the PRNP amyloid precursor gene on chromosome 20

P. Brown, D. Gajdusek, L. Cartier, 1992, Journal of the Neurological Sciences.

Codon 178 mutation in ethnically diverse Creutzfeldt-Jakob disease families

P. Brown, D. Gajdusek, D. Asher, 1991, The Lancet.

Atypical Creutzfeldt‐Jakob disease in an American family with an insert mutation in the PRNP amyloid precursor gene

W. Sheremata, P. Brown, D. Gajdusek, 1992, Neurology.

New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindred

P. Brown, D. Gajdusek, L. Goldfarb, 1991, The Lancet.