Expanding the phenotype in argininosuccinic aciduria: need for new therapies. (2017)
Attributed to:
MICA: Development of gene therapy for the incurable inherited childhood epilepsy, Dravet Syndrome
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1007/s10545-017-0022-x
PubMed Identifier: 28251416
Publication URI: http://europepmc.org/abstract/MED/28251416
Type: Journal Article/Review
Volume: 40
Parent Publication: Journal of inherited metabolic disease
Issue: 3
ISSN: 0141-8955