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APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer ... | ResearchHub
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APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases
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Authors
Hélène-Marie Lanoiselée
36 more
Hélène-Marie Lanoiselée
•
Morgane Lacour
34 more
•
Dominique Campion
Published
March 28, 2017
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Journal
PLoS Medicine
Topics
Biology
Physiology
Medicine
Internal Medicine
Pharmacology
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DOI
10.1371/journal.pmed.1002270
License
CC-BY
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Supporters
Support the authors with ResearchCoin
Tip RSC
Journal
PLoS Medicine
Topics
Biology
Physiology
Medicine
Internal Medicine
Pharmacology
Show all topics
DOI
10.1371/journal.pmed.1002270
License
CC-BY
Other Formats
PDF