De novo DNM1L mutation associated with mitochondrial epilepsy syndrome with fever sensitivity. (2018)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1212/nxg.0000000000000258

PubMed Identifier: 30109270

Publication URI: http://europepmc.org/abstract/MED/30109270

Type: Journal Article/Review

Volume: 4

Parent Publication: Neurology. Genetics

Issue: 4

ISSN: 2376-7839