TY  - JOUR
AU  - García Antón, María Teresa
AU  - Salazar Corral, Juan José
AU  - Hoz Montañana, María Rosa De
AU  - Rojas López, María Blanca
AU  - Ramírez Sebastián, Ana Isabel
AU  - Triviño Casado, Alberto
AU  - Aroca Aguilar, José Daniel
AU  - García Feijoo, Julián
AU  - Escribano, Julio
AU  - Ramírez Sebastián, José Manuel
PY  - 2017
DO  - 10.1371/journal.pone.0176386
SN  - 1932-6203
UR  - https://hdl.handle.net/20.500.14352/17809
T2  - PLoS ONE
AB  - Mutations in the CYP1B1 gene are currently the main known genetic cause of primary congenital glaucoma (PCG), a leading cause of blindness in children. Here, we analyze for the first time the CYP1B1 genotype activity and the microscopic and clinical...
LA  - eng
M2  - e0176386
PB  - Public Library Science
KW  - Mutations
KW  - PCG
KW  - Primary Congenial Glaucoma
KW  - Blindess in children
KW  - Goniodysgenesis
TI  - Goniodysgenesis variability and activity of CYP1B1 genotypes in primary congenital glaucoma
TY  - journal article
VL  - 12
ER  -