Premium
Familial prion disease with a novel serine to isoleucine mutation at codon 132 of prion protein gene ( PRNP )
Author(s) -
Hilton D. A.,
Head M. W.,
Singh V. K,
Bishop M.,
Ironside J. W.
Publication year - 2009
Publication title -
neuropathology and applied neurobiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.538
H-Index - 95
eISSN - 1365-2990
pISSN - 0305-1846
DOI - 10.1111/j.1365-2990.2008.00964.x
Subject(s) - prnp , prion protein , isoleucine , mutation , genetics , gene , biology , disease , medicine , amino acid , genotype , leucine , pathology