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ABCA7 frameshift deletion associated with Alzheimer disease in African Americans

OBJECTIVE: To identify a causative variant(s) that may contribute to Alzheimer disease (AD) in African Americans (AA) in the ATP-binding cassette, subfamily A (ABC1), member 7 (ABCA7) gene, a known risk factor for late-onset AD. METHODS: Custom capture sequencing was performed on ∼150 kb encompassin...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Τόπος έκδοσης:Neurol Genet
Κύριοι συγγραφείς: Cukier, Holly N., Kunkle, Brian W., Vardarajan, Badri N., Rolati, Sophie, Hamilton-Nelson, Kara L., Kohli, Martin A., Whitehead, Patrice L., Dombroski, Beth A., Van Booven, Derek, Lang, Rosalyn, Dykxhoorn, Derek M., Farrer, Lindsay A., Cuccaro, Michael L., Vance, Jeffery M., Gilbert, John R., Beecham, Gary W., Martin, Eden R., Carney, Regina M., Mayeux, Richard, Schellenberg, Gerard D., Byrd, Goldie S., Haines, Jonathan L., Pericak-Vance, Margaret A.
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: Wolters Kluwer 2016
Θέματα:
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4871806/
https://ncbi.nlm.nih.gov/pubmed/27231719
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000079
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