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New SMARCA2 mutation in a patient with Nicolaides-Baraitser syndrome and myoclonic astatic epilepsy. (2017)

First Author: Tang 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/10.1002/ajmg.a.37935

PubMed Identifier: 27665729

Publication URI: http://europepmc.org/abstract/MED/27665729

Type: Journal Article/Review

Volume: 173

Parent Publication: American journal of medical genetics. Part A

Issue: 1

ISSN: 1552-4825