Iarossi, G.; Sinibaldi, L.; Passarelli, C.; Coppe’, A.M.; 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, 2183.
https://doi.org/10.3390/diagnostics12092183
AMA Style
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
Chicago/Turabian Style
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
APA Style
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
