ROLE OF THE POLYMORPHISM AT CODON 129 OF THE PRION PROTEIN GENE IN THE PHENOTYPIC EXPRESSION OF GERSTMANN-STRÄUSSLER-SCHEINKER DISEASE ASSOCIATED WITH THE F198S MUTATION.

Details

Language :

English

ISSN :

00223069

Volume :

63

Issue :

5

Database :

Complementary Index

Journal :

Journal of Neuropathology & Experimental Neurology

Publication Type :

Academic Journal

Accession number :

113888135