Corrigendum to “Assessment of common variability and expression quantitative trait loci for genome-wide associations for progressive supranuclear palsy.” [Neurobiol. Aging 35 (2014) 1514.e1–1514.e12]
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Corrigendum Corrigendum to “Assessment of common variability and expression quantitative trait loci for genome-wide associations for progressive supranuclear palsy.” [Neurobiol. Aging 35 (2014) 1514.e1e1514.e12] Raffaele Ferrari, Mina Ryten, Roberto Simone, Daniah Trabzuni, Nayia Nicolaou, Geshanthi Hondhamuni, Adaikalavan Ramasamy, JanaVandrovcova, UK Brain Expression Consortium, Michael E. Weale, Andrew J. Lees, Parastoo Momeni, John Hardy, Rohan de Silva
منابع مشابه
Assessment of common variability and expression quantitative trait loci for genome-wide associations for progressive supranuclear palsy
Progressive supranuclear palsy is a rare parkinsonian disorder with characteristic neurofibrillary pathology consisting of hyperphosphorylated tau protein. Common variation defining the microtubule associated protein tau gene (MAPT) H1 haplotype strongly contributes to disease risk. A recent genome-wide association study (GWAS) revealed 3 novel risk loci on chromosomes 1, 2, and 3 that primaril...
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BACKGROUND Many genes/loci associated with Parkinsonian disorders have been identified. However, the genetic causes for a number of familial forms of Parkinsonian disorders remain to be elucidated. OBJECTIVE It was the aim of this paper to review the familial progressive supranuclear palsy (PSP) cases without any known gene mutations published in the English literature. METHODS We searched ...
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