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Mutation in the 3’untranslated region of APP as a genetic determinant of cerebral amyloid angiopathyEuropean Journal of Human Genetics, 2015, 24 (1), pp.92-98. ⟨10.1038/ejhg.2015.61⟩
Article dans une revue
hal-01234142v1
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Activating NOTCH3 mutation in a patient with small-vessel-disease of the brainHuman Mutation, 2008, 29 (3), pp.452. ⟨10.1002/humu.9527⟩
Article dans une revue
hal-00650736v1
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C9ORF72 repeat expansions in the frontotemporal dementias spectrum of diseases: a flow-chart for genetic testing.Journal of Alzheimer's Disease, 2013, 34 (2), pp.485-99. ⟨10.3233/JAD-121456⟩
Article dans une revue
hal-00924796v1
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