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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...
Αποθηκεύτηκε σε:
Τόπος έκδοσης: | Neurol Genet |
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Κύριοι συγγραφείς: | , , , , , , , , , , , , , , , , , , , , , , |
Μορφή: | Artigo |
Γλώσσα: | Inglês |
Έκδοση: |
Wolters Kluwer
2016
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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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