Familial prion disease with a novel serine to isoleucine mutation at codon 132 of prion protein gene (PRNP)

D A Hilton, M W Head, V K Singh, M Bishop, J W Ironside

Research output: Contribution to journalLetterpeer-review

Original languageEnglish
Pages (from-to)111-5
Number of pages5
JournalNeuropathology and Applied Neurobiology
Volume35
Issue number1
DOIs
Publication statusPublished - 2009

Cite this