Detalhe da pesquisa
1.
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.
Neuropediatrics
; 49(6): 373-378, 2018 12.
Artigo
Inglês
| MEDLINE | ID: mdl-30114719