xmlui.ArtifactBrowser.ConfigurableBrowse.title.metadata.subjectArtikkelit"DAP12"

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Heterozygous TYROBP deletion (PLOSLFIN) is not a strong risk factor for cognitive impairment

Kaivola, Karri; Jansson, Lilja; Saarentaus, Elmo; Kiviharju, Anna; Rantalainen, Ville; Eriksson, Johan G.; Strandberg, Timo E.; Polvikoski, Tuomo; Myllykangas, Liisa; Tienari, Pentti J.
NEUROBIOLOGY OF AGING (2018)
The C9ORF72 expansion does not affect the phenotype in Nasu-Hakola disease with the DAP12 mutation

Solje, Eino; Hartikainen, Paivi; Valori, Miko; Vanninen, Ritva; Tiihonen, Jari; Hakola, Panu; Tienari, Pentti J.; Remes, Anne M.
NEUROBIOLOGY OF AGING : 7 (28.08.2014)

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