Haplotype-specific MAPT exon 3 expression regulated by common intronic polymorphisms associated with Parkinsonian disorders. (2017)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1186/s13024-017-0224-6
PubMed Identifier: 29084565
Publication URI: http://europepmc.org/abstract/MED/29084565
Type: Journal Article/Review
Volume: 12
Parent Publication: Molecular neurodegeneration
Issue: 1
ISSN: 1750-1326