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Coding mutations in SORL1 and Alzheimer’s disease
IMPORTANCE: Common single nucleotide polymorphisms in the SORL1 gene have been associated with late onset Alzheimer’s disease (LOAD) but causal variants have not been fully characterized nor has the mechanism been established. OBJECTIVE: To identify functional SORL1 mutations in patients with LOAD....
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| Publicat a: | Ann Neurol |
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| Autors principals: | , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4367199/ https://ncbi.nlm.nih.gov/pubmed/25382023 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ana.24305 |
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