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Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation
OBJECTIVE: To generate a clinical and pathologic phenotype of patients carrying rare loss-of-function mutations in ABCA7, identified in a Belgian Alzheimer patient cohort and in an autosomal dominant family. METHODS: We performed a retrospective review of available data records, medical records, res...
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| Publicat a: | Neurology |
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| Autors principals: | , , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Lippincott Williams & Wilkins
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4917260/ https://ncbi.nlm.nih.gov/pubmed/27037232 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0000000000002628 |
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