Celma Nos, F.; Hernández, G.; Ferrer-Cortès, X.; Hernandez-Rodriguez, I.; Navarro-Almenzar, B.; Fuster, J.L.; Bermúdez Cortés, M.; Pérez-Montero, S.; Tornador, C.; Sanchez, M.
Hereditary Hyperferritinemia Cataract Syndrome: Ferritin L Gene and Physiopathology behind the Disease—Report of New Cases. Int. J. Mol. Sci. 2021, 22, 5451.
https://doi.org/10.3390/ijms22115451
AMA Style
Celma Nos F, Hernández G, Ferrer-Cortès X, Hernandez-Rodriguez I, Navarro-Almenzar B, Fuster JL, Bermúdez Cortés M, Pérez-Montero S, Tornador C, Sanchez M.
Hereditary Hyperferritinemia Cataract Syndrome: Ferritin L Gene and Physiopathology behind the Disease—Report of New Cases. International Journal of Molecular Sciences. 2021; 22(11):5451.
https://doi.org/10.3390/ijms22115451
Chicago/Turabian Style
Celma Nos, Ferran, Gonzalo Hernández, Xènia Ferrer-Cortès, Ines Hernandez-Rodriguez, Begoña Navarro-Almenzar, José Luis Fuster, Mar Bermúdez Cortés, Santiago Pérez-Montero, Cristian Tornador, and Mayka Sanchez.
2021. "Hereditary Hyperferritinemia Cataract Syndrome: Ferritin L Gene and Physiopathology behind the Disease—Report of New Cases" International Journal of Molecular Sciences 22, no. 11: 5451.
https://doi.org/10.3390/ijms22115451
APA Style
Celma Nos, F., Hernández, G., Ferrer-Cortès, X., Hernandez-Rodriguez, I., Navarro-Almenzar, B., Fuster, J. L., Bermúdez Cortés, M., Pérez-Montero, S., Tornador, C., & Sanchez, M.
(2021). Hereditary Hyperferritinemia Cataract Syndrome: Ferritin L Gene and Physiopathology behind the Disease—Report of New Cases. International Journal of Molecular Sciences, 22(11), 5451.
https://doi.org/10.3390/ijms22115451
