A defect in the retromer accessory protein, SNX27, manifests by infantile myoclonic epilepsy and neurodegeneration. (2015)
Attributed to:
Defining the mechanistic and functional details of an evolutionarily conserved non-canonical retromer pathway.
funded by
BBSRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1007/s10048-015-0446-0
PubMed Identifier: 25894286
Publication URI: http://europepmc.org/abstract/MED/25894286
Type: Journal Article/Review
Volume: 16
Parent Publication: Neurogenetics
Issue: 3
ISSN: 1364-6745