Novel APP mutation V715A associated with presenile Alzheimer's disease in a German family [2]

Marc Cruts, Bart Dermaut, Rosa V Rademakers, Marleen Van Den Broeck, Florian Stögbauer, Christine Van Broeckhoven

Research output: Contribution to journalArticle

14 Citations (Scopus)
Original languageEnglish (US)
Pages (from-to)1374-1375
Number of pages2
JournalJournal of Neurology
Volume250
Issue number11
DOIs
StatePublished - Nov 2003
Externally publishedYes

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DNA Mutational Analysis
Amyloid beta-Protein Precursor
Pedigree
Restriction Fragment Length Polymorphisms
Germany
Alzheimer Disease
Mutation

ASJC Scopus subject areas

  • Clinical Neurology
  • Neurology

Cite this

Novel APP mutation V715A associated with presenile Alzheimer's disease in a German family [2]. / Cruts, Marc; Dermaut, Bart; Rademakers, Rosa V; Van Den Broeck, Marleen; Stögbauer, Florian; Van Broeckhoven, Christine.

In: Journal of Neurology, Vol. 250, No. 11, 11.2003, p. 1374-1375.

Research output: Contribution to journalArticle

Cruts, M, Dermaut, B, Rademakers, RV, Van Den Broeck, M, Stögbauer, F & Van Broeckhoven, C 2003, 'Novel APP mutation V715A associated with presenile Alzheimer's disease in a German family [2]', Journal of Neurology, vol. 250, no. 11, pp. 1374-1375. https://doi.org/10.1007/s00415-003-0182-5
Cruts, Marc ; Dermaut, Bart ; Rademakers, Rosa V ; Van Den Broeck, Marleen ; Stögbauer, Florian ; Van Broeckhoven, Christine. / Novel APP mutation V715A associated with presenile Alzheimer's disease in a German family [2]. In: Journal of Neurology. 2003 ; Vol. 250, No. 11. pp. 1374-1375.
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