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. 2016 Oct 12;11:1433–1440. doi: 10.2147/CIA.S111821

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© 2016 Bagyinszky et al. This work is published and licensed by Dove Medical Press Limited

The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.

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Data of genetic analysis for the AD patient with PSEN1 L226F.

Notes: (A) SSCP data of patient with L226F mutation, located at position 2 (2*). Numbers 1, 3, and 4 are wild-type samples (B). Sequencing data of PSEN1 L226F. (C) Location of L226F in PSEN1 protein.

Abbreviations: SSCP, single strand conformation polymorphism; AD, Alzheimer’s disease.