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Tag Archives: University Medical Center Hamburg-Eppendorf
Genetic Mutation Which Delays Alzheimer’s Disease? (NHS Choices / Molecular Psychiatry)
Summary A study of 71 persons from an extended family (comprising around 5,000 people) in northern Colombia, who carry a mutation in a gene called PSEN1 (the so-called the Paisa mutation, which causes a rare, severe form of early-onset Alzheimer’s disease), … Continue reading
Posted in For Researchers (mostly), In the News, International, NHS Digital (Previously NHS Choices), Quick Insights, Statistics, Universal Interest
Tagged Alzheimer's Disease Susceptibility Genes, ApoE e4 Allele, APOE-4 Allele, Apoe-ε4 Allele, Apolipoprotein E (APOE) e4 Allele, Australia, Australian National University, Behind the Headlines, Biomolecular Resource Facility: Australian National University, Colombia, Department of Genome Sciences: Australian National University, Early Mammalian Development Laboratory: Australian National University, Early-Onset Alzheimer's Gene, Flinders University (Australia), Genetic Research, Genetic Susceptibility Loci, Genetic Triggers, Genetic Variants, Genetic Variation (APOE*E2 Allele), Genetics, Genetics of Alzheimer's Disease, Genome Diversity and Health Group: Australian National University, Genomics and Predictive Medicine Group: Australian National University, Germany, Hamburg, Hereditary Form of Early-Onset Alzheimer's Disease, Institute of Neuropathology: University Medical Center Hamburg-Eppendorf, John Curtin School of Medical Research: Australian National University, Mental Health Research Center at Eastern State Hospital: University of Kentucky, Molecular Psychiatry (Journal), Nathan Kline Institute for Psychiatric Research, Nathan Kline Institute for Psychiatric Research (USA), Neurodegeneration, Neurodegenerative Disease Research, Neurodegenerative Diseases, Neuroscience Research Group: University of Antioquia, New York University, Northern Colombia, NYU Child Study Center: NYU Langone Medical Center, NYU Langone Medical Center, Paisa Mutation: Mutated PSEN1 Gene, Presenilin 1 (PSEN1), Presenilin 1 Mutation (PSEN1), PSEN1 E280A Alzheimer's Disease, PSEN1 E280A Carriers, PSEN1: Presenilin 1 Mutation, Rare Unusual Hereditary Form of Alzheimer’s Disease, Research School of Biology: Australian National University, School of Medicine: Flinders University, South Australian Health and Medical Research Institute and Department of Psychiatry: Flinders University, University Medical Center Hamburg-Eppendorf, University of Antioquia (Colombia), University of Antioquia in Colombia, University of Kentucky, USA
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