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Iarossi G, Sinibaldi L, Passarelli C, Coppe’ AM, Cappelli A, Petrocelli G, Catena G, Perrone C, Falsini B, Novelli A, et al. A Novel Autosomal Recessive Variant of the NRL Gene Causing Enhanced S-Cone Syndrome: A Morpho-Functional Analysis of Two Unrelated Pediatric Patients. Diagnostics. 2022; 12(9):2183. https://doi.org/10.3390/diagnostics12092183

Iarossi, Giancarlo, Lorenzo Sinibaldi, Chiara Passarelli, Andrea Maria Coppe’, Alessandro Cappelli, Gianni Petrocelli, Gino Catena, Chiara Perrone, Benedetto Falsini, Antonio Novelli, and et al. 2022. "A Novel Autosomal Recessive Variant of the NRL Gene Causing Enhanced S-Cone Syndrome: A Morpho-Functional Analysis of Two Unrelated Pediatric Patients" Diagnostics 12, no. 9: 2183. https://doi.org/10.3390/diagnostics12092183

Iarossi, G., Sinibaldi, L., Passarelli, C., Coppe’, A. M., Cappelli, A., Petrocelli, G., Catena, G., Perrone, C., Falsini, B., Novelli, A., Bartuli, A., & Buzzonetti, L. (2022). A Novel Autosomal Recessive Variant of the NRL Gene Causing Enhanced S-Cone Syndrome: A Morpho-Functional Analysis of Two Unrelated Pediatric Patients. Diagnostics, 12(9), 2183. https://doi.org/10.3390/diagnostics12092183