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-...

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Detalles Bibliográficos
Autores principales: Ferrari, Raffaele, Ryten, Mina, Simone, Roberto, Trabzuni, Daniah, Nicolaou, Naiya, Hondhamuni, Geshanthi, Ramasamy, Adaikalavan, Vandrovcova, Jana, Weale, Michael E., Lees, Andrew J., Momeni, Parastoo, Hardy, John, de Silva, Rohan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Genetic Report Abstract
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4104112/
https://www.ncbi.nlm.nih.gov/pubmed/24503276
http://dx.doi.org/10.1016/j.neurobiolaging.2014.01.010

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