Heterogeneity of FHF1 related phenotype: Novel case with early onset severe attacks of apnea, partial mitochondrial respiratory chain complex II deficiency, neonatal onset seizures without neurodegeneration

Published 2017 View Full Article

Authors

Keywords

Early onset epileptic encephalopathy, Genetics, Children, EEG, Seizure

Journal

EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

Volume 21, Issue 5, Pages 783-786

Publisher

Elsevier BV

Online

2017-04-29

DOI

10.1016/j.ejpn.2017.04.001

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