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Article

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

Neuropathology and applied neurobiology - 1 Feb 2009

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

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 19187063
DOI: 10.1111/j.1365-2990.2008.00964.x

Genes

PRNP

Provenance

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Polymorphism at codon 129 or codon 219 of PRNP and clinical heterogeneity in a previously unreported family with Gerstmann-Sträussler-Scheinker disease (PrP-P102L mutation).Semantic proximity Read ↗

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