Invernizzi F, Zorzi G, Legati A, Coppola G, d'Adamo P, Nardocci N, Garavaglia B, Ghezzi D. Benign hereditary chorea and deletions outside NKX2-1: What's the role of MBIP?. Eur J Med Genet 2018;61(10):581-584.

Ghezzi D, Sevrioukova I, Invernizzi F, Lamperti C, Mora M, d'Adamo P, Novara F, Zuffardi O, Uziel G, Zeviani M. Severe X-linked mitochondrial encephalomyopathy associated with a mutation in apoptosis-inducing factor. Am J Hum Genet 2010;86(4):639-49.