Clinical and molecular characterisation of a Parkinson family with a novel PINK1 mutation.
Prestel J; Gempel K; Hauser TK; Schweitzer K; Prokisch H; Ahting U; Freudenstein D; Bueltmann E; Naegele T; Berg D; Klopstock T; Gasser T; Journal Of Neurology, 2008, vol. 255, issue 5, p 643, ISSN 03405354. ISBN 03405354.

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