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A defect in the retromer accessory protein, SNX27, manifests by infantile myoclonic epilepsy and neurodegeneration. (2015)

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