Myoclonic epilepsy with ragged red fibers syndrome mimicking myotonic dystrophy type 2: The need of genetic diagnosis

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Bibliographic Details
Published in:Neuromuscular disorders : NMD 2016-10, Vol.26, p.S177-S177
Main Authors: Lusakowska, A, Tonska, K, Sulek, A, Krysa, W, Szmidt-Salkowska, E, Kaminska, A
Format: Article
Language:English
Subjects:
Neurology
Online Access:Get full text
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ISSN:0960-8966
DOI:10.1016/j.nmd.2016.06.330