bibliographic entry 213447 [be/213447]
https://w3id.org/oc/corpus/be/213447

is a
content
  • Coppola, G, Chinnathambi, S, Lee, JJ, Dombroski, BA, Baker, MC, Soto-Ortolaza, AI, Lee, SE, Klein, E, Huang, AY, Sears, R. Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer’s diseases, Hum Mol Genet, 2012, 21, 3500, 3512, DOI: 10.1093/hmg/dds161, PMID: 22556362
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