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Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS. (2013)

First Author: Kim HJ

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

PubMed Identifier: 23455423

Publication URI: http://europepmc.org/abstract/MED/23455423

Type: Journal Article/Review

Volume: 495

Parent Publication: Nature

Issue: 7442

ISSN: 0028-0836