App, psen1, and psen2 mutations in early-onset alzheimer disease: a genetic screening study of familial and sporadic cases

HIGHLIGHTS

• who: H#_#x00E9 and collaborators from the , and Rouen University, Department of Neurology and Centre Hospitalier du Rouvray, Sotteville-lès-Rouen, France have published the article: APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases, in the Journal: (JOURNAL) of March/28,/2017
• what: The authors report here novel update of the genetic screening of the large AD-EOAD series ascertained across 28 French hospitals from 1993 onwards bringing the total number of families with identified mutations to n = 170. The aim of . . .
  

   

  

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