Novel Missense Mutation A789V in IQSEC2 Underlies X-Linked Intellectual Disability in the MRX78 Family. (2015)

First Author: Kalscheuer VM
Attributed to:  The role of NMDA receptor dysfunction in epileptic disorders funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.3389/fnmol.2015.00085

PubMed Identifier: 26793055

Publication URI: http://europepmc.org/abstract/MED/26793055

Type: Journal Article/Review

Volume: 8

Parent Publication: Frontiers in molecular neuroscience

ISSN: 1662-5099