المؤلفون: M. C. Zanellati, V. Monti, C. Barzaghi, C. Reale, N. Nardocci, A. Albanese, E. M. Valente, B. Garavaglia, D. Ghezzi

المساهمون: M.C. Zanellati, V. Monti, C. Barzaghi, C. Reale, N. Nardocci, A. Albanese, E.M. Valente, D. Ghezzi, B. Garavaglia

مصطلحات موضوعية: mitochondrial dynamic, mitochondrial membrane potential, oxygen consumption, park2, parkin, genetic, molecular medicine, genetics (clinical), Settore MED/03 - Genetica Medica, Settore BIO/11 - Biologia Molecolare

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/25815004; info:eu-repo/semantics/altIdentifier/wos/WOS:000352766800001; volume:6; issue:MAR; numberofpages:9; journal:FRONTIERS IN GENETICS; http://hdl.handle.net/2434/523733Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84927135557

الإتاحة: https://doi.org/10.3389/fgene.2015.00078Test
http://hdl.handle.net/2434/523733Test

المؤلفون: L. Melchionda, N. S. Damseh, B. Y. Abu Libdeh, A. Nasca, O. Elpeleg, A. Zanolini, D. Ghezzi

المساهمون: L. Melchionda, N.S. Damseh, B.Y. Abu Libdeh, A. Nasca, O. Elpeleg, A. Zanolini, D. Ghezzi

مصطلحات موضوعية: bilateral basal ganglia lesion, complex iii deficiency, encephalomyopathy, mitochondrial disease, novel mutation, Ttc19, genetic, molecular medicine, genetics (clinical), Settore MED/03 - Genetica Medica

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/25452764; info:eu-repo/semantics/altIdentifier/wos/WOS:000347941100001; volume:5; issue:NOV; numberofpages:5; journal:FRONTIERS IN GENETICS; http://hdl.handle.net/2434/523758Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84917742690

الإتاحة: https://doi.org/10.3389/fgene.2014.00397Test
http://hdl.handle.net/2434/523758Test

المؤلفون: F. Invernizzi, A. Ardissone, E. Lamantea, B. Garavaglia, M. Zeviani, L. Farina, I. Moroni, D. Ghezzi

المساهمون: F. Invernizzi, A. Ardissone, E. Lamantea, B. Garavaglia, M. Zeviani, L. Farina, D. Ghezzi, I. Moroni

مصطلحات موضوعية: Brain MRI, leukoencephalopathy, mitochondrial disorder, MMDS1, multiple mitochondrial dysfunction syndrome, NFU1, genetic, molecular medicine, genetics (clinical), Settore MED/03 - Genetica Medica, Settore MED/26 - Neurologia

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/25477904; info:eu-repo/semantics/altIdentifier/wos/WOS:000347942700001; volume:5; issue:NOV; journal:FRONTIERS IN GENETICS; http://hdl.handle.net/2434/523776Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84917736963

الإتاحة: https://doi.org/10.3389/fgene.2014.00412Test
http://hdl.handle.net/2434/523776Test

المؤلفون: Frascarelli C., Zanetti N., Nasca A., Izzo R., Lamperti C., Lamantea E., Legati A., Ghezzi D.

المساهمون: C. Frascarelli, N. Zanetti, A. Nasca, R. Izzo, C. Lamperti, E. Lamantea, A. Legati, D. Ghezzi

مصطلحات موضوعية: MinION, complex-rearrangement, long read, macrodeletion, mtDNA, multiple deletion, oxford nanopore, structural variants, Settore MED/03 - Genetica Medica, Settore BIO/18 - Genetica

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/37456669; info:eu-repo/semantics/altIdentifier/wos/WOS:001029313700001; volume:14; firstpage:1; lastpage:17; numberofpages:17; journal:FRONTIERS IN GENETICS; https://hdl.handle.net/2434/993816Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85165061839

الإتاحة: https://doi.org/10.3389/fgene.2023.1089956Test
https://hdl.handle.net/2434/993816Test