Home
About
Overview
Sharing Data
ORCID
Help
History (68)
Sublytic complement attack reduces infarct size in rabbit isolated hearts: evidence for C5a-mediated cardioprotection.
Removal of EPI Nyquist ghost artifacts with two-dimensional phase correction.
Consumers' perceptions about risk of and access to nonprescription medications.
Personality dimensions and disorders in pathological gambling.
Mutation of the prion protein gene at codon 208 in familial Creutzfeldt-Jakob disease.
See All 68 Pages
Find People
Find Everything
Login
to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
0
)
Return to Top
Mutation of the prion protein gene at codon 208 in familial Creutzfeldt-Jakob disease.
Mutation of the prion protein gene at codon 208 in familial Creutzfeldt-Jakob disease. Neurology. 1996 Nov; 47(5):1305-12.
View in:
PubMed
subject areas
Base Sequence
Creutzfeldt-Jakob Syndrome
Humans
Male
Middle Aged
Molecular Sequence Data
Mutation
Pedigree
Prions
authors with profiles
James Mastrianni