L. MELCHIONDA Et Al. , "Mutations in APOPT1, Encoding a Mitochondria! Protein, Cause Cavitating Leukoencephalopathy with Cytochrome c Oxidase Deficiency," AMERICAN JOURNAL OF HUMAN GENETICS , vol.95, no.3, pp.315-325, 2014
MELCHIONDA, L. Et Al. 2014. Mutations in APOPT1, Encoding a Mitochondria! Protein, Cause Cavitating Leukoencephalopathy with Cytochrome c Oxidase Deficiency. AMERICAN JOURNAL OF HUMAN GENETICS , vol.95, no.3 , 315-325.
MELCHIONDA, L., HAACK, T. B., HARDY, S., Abbink, T. E. M., FERNANDEZ-VIZARRA, E., LAMANTEA, E., ... MARCHET, S.(2014). Mutations in APOPT1, Encoding a Mitochondria! Protein, Cause Cavitating Leukoencephalopathy with Cytochrome c Oxidase Deficiency. AMERICAN JOURNAL OF HUMAN GENETICS , vol.95, no.3, 315-325.
MELCHIONDA, Laura Et Al. "Mutations in APOPT1, Encoding a Mitochondria! Protein, Cause Cavitating Leukoencephalopathy with Cytochrome c Oxidase Deficiency," AMERICAN JOURNAL OF HUMAN GENETICS , vol.95, no.3, 315-325, 2014
MELCHIONDA, Laura Et Al. "Mutations in APOPT1, Encoding a Mitochondria! Protein, Cause Cavitating Leukoencephalopathy with Cytochrome c Oxidase Deficiency." AMERICAN JOURNAL OF HUMAN GENETICS , vol.95, no.3, pp.315-325, 2014
MELCHIONDA, L. Et Al. (2014) . "Mutations in APOPT1, Encoding a Mitochondria! Protein, Cause Cavitating Leukoencephalopathy with Cytochrome c Oxidase Deficiency." AMERICAN JOURNAL OF HUMAN GENETICS , vol.95, no.3, pp.315-325.
@article{article, author={Laura MELCHIONDA Et Al. }, title={Mutations in APOPT1, Encoding a Mitochondria! Protein, Cause Cavitating Leukoencephalopathy with Cytochrome c Oxidase Deficiency}, journal={AMERICAN JOURNAL OF HUMAN GENETICS}, year=2014, pages={315-325} }