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Severe infantile epileptic encephalopathy due to mutations in PLCB1: expansion of the genotypic and phenotypic disease spectrum. (2014)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1111/dmcn.12450

PubMed Identifier: 24684524

Publication URI: http://europepmc.org/abstract/MED/24684524

Type: Journal Article/Review

Volume: 56

Parent Publication: Developmental medicine and child neurology

Issue: 11

ISSN: 0012-1622