Priglinger, C.S.; Gerhardt, M.J.; Priglinger, S.G.; Schaumberger, M.; Neuhann, T.M.; Bolz, H.J.; Mehraein, Y.; Rudolph, G.
Phenotypic and Genetic Spectrum in 309 Consecutive Pediatric Patients with Inherited Retinal Disease. Int. J. Mol. Sci. 2024, 25, 12259.
https://doi.org/10.3390/ijms252212259
AMA Style
Priglinger CS, Gerhardt MJ, Priglinger SG, Schaumberger M, Neuhann TM, Bolz HJ, Mehraein Y, Rudolph G.
Phenotypic and Genetic Spectrum in 309 Consecutive Pediatric Patients with Inherited Retinal Disease. International Journal of Molecular Sciences. 2024; 25(22):12259.
https://doi.org/10.3390/ijms252212259
Chicago/Turabian Style
Priglinger, Claudia S., Maximilian J. Gerhardt, Siegfried G. Priglinger, Markus Schaumberger, Teresa M. Neuhann, Hanno J. Bolz, Yasmin Mehraein, and Guenther Rudolph.
2024. "Phenotypic and Genetic Spectrum in 309 Consecutive Pediatric Patients with Inherited Retinal Disease" International Journal of Molecular Sciences 25, no. 22: 12259.
https://doi.org/10.3390/ijms252212259
APA Style
Priglinger, C. S., Gerhardt, M. J., Priglinger, S. G., Schaumberger, M., Neuhann, T. M., Bolz, H. J., Mehraein, Y., & Rudolph, G.
(2024). Phenotypic and Genetic Spectrum in 309 Consecutive Pediatric Patients with Inherited Retinal Disease. International Journal of Molecular Sciences, 25(22), 12259.
https://doi.org/10.3390/ijms252212259