Horm Piseth
发表
R. Casson,
D. Selva,
W. Chan,
2012,
Ophthalmic epidemiology.
Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma.
Colin A. Johnson,
G. Taylor,
J. Craig,
2011,
American journal of human genetics.
D. Selva,
J. Muecke,
D. Sia,
2010,
Ophthalmic epidemiology.