Lan MY, Liu JS, Wu YS, Peng CH, Chang YY. A novel APP mutation (D678H) in a Taiwanese patient exhibiting dementia and cerebral microvasculopathy. J Clin Neurosci. 2014 Mar;21(3):513-5. Epub 2013 Aug 6 PubMed.

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Mutations

  1. APP D678H (Taiwanese)