TY  - JOUR 
AU  - Álvarez de Toledo Elizalde, J.
AU  - López García, S.
AU  - Benítez del Castillo, J.M.
AU  - Durán de la Colina, J.
AU  - Gris Castejón, O.
AU  - Celis Sánchez, J.
AU  - Herreras Cantalapiedra, José María
PY  - 2021
SN  - 2173-5794
UR  - https://uvadoc.uva.es/handle/10324/82872
AB  - Congenital aniridia is a multisystemic genetic disease due to a mutation in PAX6 gene which severely affects the development and functionality of the human eyes. In patients affected by the mutation, aside from the absence or defects of iris tissue...
LA  - eng
PB  - Elsevier
KW  - Congenital aniridia
KW  - Keratopathy
KW  - Limbal stem cell transplantation
KW  - Keratoplasty
KW  - Keratoprostheses
KW  - Limbal stem cell culture
KW  - Mesenchymal cell culture
TI  - Aniridia and the ocular surface: Medical and surgical problems and solutions
DO  - 10.1016/j.oftale.2021.04.003
ER  -