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
Issue number1
Publication statusPublished - 2009

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