Bianco, A., Bisceglia, L., De Caro, M. F., Galeandro, V., De Bonis, P., Tullo, A., . . . Petruzzella, V. (2018). Leber’s hereditary optic neuropathy, intellectual disability and epilepsy presenting with variable penetrance associated to the m.3460G >A mutation and a heteroplasmic expansion of the microsatellite in MTRNR1 gene – case report. BMC Med Genet.

Bianco, Angelica, Luigi Bisceglia, Maria Fara De Caro, Valeria Galeandro, Patrizia De Bonis, Apollonia Tullo, Stefano Zoccolella, Silvana Guerriero, et Vittoria Petruzzella. "Leber’s Hereditary Optic Neuropathy, Intellectual Disability and Epilepsy Presenting With Variable Penetrance Associated to the M.3460G >A Mutation and a Heteroplasmic Expansion of the Microsatellite in MTRNR1 Gene – Case Report." BMC Med Genet 2018.

Bianco, Angelica, et al. "Leber’s Hereditary Optic Neuropathy, Intellectual Disability and Epilepsy Presenting With Variable Penetrance Associated to the M.3460G >A Mutation and a Heteroplasmic Expansion of the Microsatellite in MTRNR1 Gene – Case Report." BMC Med Genet 2018.