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 |
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Zdroj: | Movement Disorders; Jul2017, Vol. 32 Issue 7, p1108-1110, 4p |
Databáze: | Complementary Index |
Externí odkaz: |