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HTRA2 Defect: A Recognizable Inborn Error of Metabolism with 3-Methylglutaconic Aciduria as Discriminating Feature Characterized by Neonatal Movement Disorder and Epilepsy—Report of 11 Patients
Kovacs-Nagy, Reka, Morin, Gilles, Nouri, Maria, Brandau, Oliver, Saadi, Nebal, Nouri, Mohammed, van den Broek, Florence, Prokisch, Holger, Mayr, Johannes, Wortmann, SaskiaLanguage:
english
Journal:
Neuropediatrics
DOI:
10.1055/s-0038-1667345
Date:
August, 2018
File:
PDF, 205 KB
english, 2018