Inherited prion disease with six octapeptide repeat insertional mutation—molecular analysis of phenotypic heterogeneity.
Simon Mead; Mark Poulter; Jon Beck; Thomas E. F. Webb; Tracy A. Campbell; Jacqueline M. Linehan; Melanie Desbruslais; Susan Joiner; Jonathan D. F. Wadsworth; Andrew King; Peter Lantos; John Collinge; Brain: A Journal of Neurology, 2006, vol. 129, issue 9, p 2297, ISSN 00068950. ISBN 14602156.

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