TY  - JOUR
AU  - Morales Fernández, Laura
AU  - Martínez De La Casa Fernández-Borrella, José María
AU  - García Bella, Javier
AU  - Méndez Hernández, Carmen D.
AU  - Saenz Frances, Federico
AU  - García Antón, Maite
AU  - Escribano, Julio
AU  - García Feijoo, Julián
DA  - Received May 15, 2013; Accepted March 11, 2014
PY  - 2015
DO  - 10.1097/IJG.0000000000000067
SN  - 1057-0829
UR  - https://hdl.handle.net/20.500.14352/23120
T2  - Journal of Glaucoma
AB  - Background: Primary congenital glaucoma (PCG) is a rare disease. In around a third of Spanish patients, the disease is attributed to mutations in the CYP1B1 gene inherited in an autosomal recessive manner. Such mutations are the main known genetic...
LA  - eng
M2  - 630
PB  - Wolters Kluwer Health
KW  - Primary congenital glaucoma
KW  - CYP1B1 gene
KW  - Genotype-phenotype
TI  - Clinical Variability of Primary Congenital Glaucoma in a Spanish Family With Cyp1b1 Gene Mutations
TY  - journal article
VL  - 24
ER  -