Michael Mullan is an English-American researcher in Alzheimer’s disease and related neurodegenerative disorders. Mullan was a co-discoverer of genetic causes of Alzheimer’s disease. Subsequently, he was a co-inventor on the original patents that covered three mutations in the amyloid precursor protein (APP) gene, a gene which is linked to familial Alzheimer’s disease. He also co-authored articles in Nature and Nature Genetics, describing these three genetic errors; he was the senior author on two of those articles. Dr. Mullan co-discovered a specific genetic mutation, which became known as “the Swedish Mutation,” because it was originally identified in DNA samples from two Swedish families whose members often developed early-onset Alzheimer’s disease. These human genetic mutations were integrated into mouse DNA to create strains of mice (transgenic animal models) that are being used worldwide to develop new drug treatments for Alzheimer’s disease.
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