Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneity.
Mead S; Poulter M; Beck J; Webb TE; Campbell TA; Linehan JM; Desbruslais M; Joiner S; Wadsworth JD; King A; Lantos P; Collinge J; Brain: A Journal Of Neurology, 2006, vol. 129, issue Pt 9, p 2297, ISSN 14602156. ISBN 14602156.

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