Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia (2017)
Attributed to:
Exosomal protein deficiencies: how abnormal RNA metabolism results in childhood-onset neurological diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/brain/awx095
Publication URI: http://dx.doi.org/10.1093/brain/awx095
Type: Journal Article/Review
Parent Publication: Brain
Issue: 6