Cruts M, Dermaut B, Rademakers R, Van den Broeck M, Stögbauer F, Van Broeckhoven C. Novel APP mutation V715A associated with presenile Alzheimer's disease in a German family. J Neurol. 2003 Nov;250(11):1374-5. PubMed.

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Mutations

  1. APP V715A (German)