Severe infantile parkinsonism because of a de novo mutation on DLP1 mitochondrial-peroxisomal protein.

Autor: Díez, H., Cortès‐Saladelafont, E., Ormazábal, A., Marmiese, A. Fernández, Armstrong, J., Matalonga, Leslie, Bravo, Miren, Briones, Paz, Emperador, Sonia, Montoya, Julio, Artuch, Rafael, Giros, Marisa, Garcia‐Cazorla, Àngels, Díez, H, Cortès-Saladelafont, E, Ormazábal, A, Marmiese, A Fernández, Garcia-Cazorla, Àngels
Zdroj: Movement Disorders; Jul2017, Vol. 32 Issue 7, p1108-1110, 4p
Databáze: Complementary Index