Baderna, V., Schultz, J., Kearns, L. S., Fahey, M., Thompson, B. A., Ruddle, J. B., . . . Maltecca, F. (2020). A novel AFG3L2 mutation close to AAA domain leads to aberrant OMA1 and OPA1 processing in a family with optic atrophy. Acta Neuropathol Commun.

Baderna, Valentina, Joshua Schultz, Lisa S. Kearns, Michael Fahey, Bryony A. Thompson, Jonathan B. Ruddle, Aamira Huq, and Francesca Maltecca. "A Novel AFG3L2 Mutation Close to AAA Domain Leads to Aberrant OMA1 and OPA1 Processing in a Family With Optic Atrophy." Acta Neuropathol Commun 2020.

Baderna, Valentina, et al. "A Novel AFG3L2 Mutation Close to AAA Domain Leads to Aberrant OMA1 and OPA1 Processing in a Family With Optic Atrophy." Acta Neuropathol Commun 2020.