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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Vydáno v:Mol Neurodegener
Hlavní autoři: Lai, Mang Ching, Bechy, Anne-Laure, Denk, Franziska, Collins, Emma, Gavriliouk, Maria, Zaugg, Judith B., Ryan, Brent J., Wade-Martins, Richard, Caffrey, Tara M.
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2017
Témata:
Research Article
On-line přístup: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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