Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS (2013)
Attributed to:
RNA processing proteins and neurodegeneration: exploring mechanisms and modelling disease
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1038/nature11922
Publication URI: http://dx.doi.org/10.1038/nature11922
Type: Journal Article/Review
Parent Publication: Nature
Issue: 7442