Φορτώνει......
Role of common and rare APP DNA sequence variants in Alzheimer disease
OBJECTIVES: More than 30 different rare mutations, including copy number variants (CNVs), in the amyloid precursor protein gene (APP) cause early-onset familial Alzheimer disease (EOFAD), whereas the contribution of common APP variants to disease risk remains controversial. In this study we systemat...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , , , , , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Lippincott Williams & Wilkins
2012
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3324321/ https://ncbi.nlm.nih.gov/pubmed/22491860 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0b013e3182515972 |
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