Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a Sephardic Jewish family.
Casali C, Bonifati V, Santorelli FM, Casari G, Fortini D, Patrignani A, Fabbrini G, Carrozzo R, D'Amati G, Locuratolo N, Vanacore N, Damiano M, Pierallini A, Pierelli F, Amabile GA, Meco G.
Casali C, et al. Among authors: fortini d, d amati g.
Neurology. 2001 Mar 27;56(6):802-5. doi: 10.1212/wnl.56.6.802.
Neurology. 2001.
PMID: 11274324