Haplotype-specific MAPT exon 3 expression regulated by common intronic polymorphisms associated with Parkinsonian disorders

BACKGROUND: Genome wide association studies have identified microtubule associated protein tau (MAPT) H1 haplotype single nucleotide polymorphisms (SNPs) as leading common risk variants for Parkinson’s disease, progressive supranuclear palsy and corticobasal degeneration. The MAPT risk variants fall...

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Publicado en:Mol Neurodegener
Main Authors: Lai, Mang Ching, Bechy, Anne-Laure, Denk, Franziska, Collins, Emma, Gavriliouk, Maria, Zaugg, Judith B., Ryan, Brent J., Wade-Martins, Richard, Caffrey, Tara M.
Formato: Artigo
Idioma:Inglês
Publicado: BioMed Central 2017
Assuntos:
Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC5663040/
https://ncbi.nlm.nih.gov/pubmed/29084565
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13024-017-0224-6
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