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Clinical spectrum of STX1B-related epileptic disorders. (2019)

First Author: Wolking S

Attributed to: Investigating the phenotype and genetic architecture of myoclonic astatic epilepsy funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1212/wnl.0000000000007089

PubMed Identifier: 30737342

Publication URI: http://europepmc.org/abstract/MED/30737342

Type: Journal Article/Review

Volume: 92

Parent Publication: Neurology

Issue: 11

ISSN: 0028-3878