reference/7995950

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/7995950

Outgoing Links

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publicationName	PLoS ONE
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bibliographicCitation	Cruchaga C, Haller G, Chakraverty S, Mayo K, Vallania FL, Mitra RD, Faber K, Williamson J, Bird T, Diaz-Arrastia R, Foroud TM, Boeve BF, Graff-Radford NR, St Jean P, Lawson M, Ehm MG, Mayeux R, Goate AM; NIA-LOAD/NCRAD Family Study Consortium. Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families. PLoS One. 2012;7(2):e31039. PMID: 22312439; PMCID: PMC3270040.
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date	2012-02-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1371/journal.pone.0031039 https://doi.org/10.1371/annotation/c92e16da-7733-421d-b063-1db19488daa6 https://pubmed.ncbi.nlm.nih.gov/PMC3270040 https://pubmed.ncbi.nlm.nih.gov/22312439
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language	English
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title	Correction: Rare Variants in APP, PSEN1 and PSEN2 Increase Risk for AD in Late-Onset Alzheimer's Disease Families
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Total number of triples: 98.