|  Help  |  About  |  Contact Us

Publication : Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma.

First Author  Khan K Year  2011
Journal  Am J Hum Genet Volume  89
Issue  3 Pages  464-73
PubMed ID  21907015 Mgi Id 
Quick Links:
 
Quick Links:
 

Expression

Publication --> Expression annotations

 

Other

1 Bio Entities

Trail: Publication

0 Expression