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

✍ Scribed by D. A. Hilton; M. W. Head; V. K Singh; M. Bishop; J. W. Ironside

Book ID: 110852608
Publisher: John Wiley and Sons
Year: 2009
Tongue: English
Weight: 298 KB
Volume: 35
Category: Article
ISSN: 0305-1846
DOI: 10.1111/j.1365-2990.2008.00964.x

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