|  Help  |  About  |  Contact Us

Publication : Mutations in TRPM1 are a common cause of complete congenital stationary night blindness.

First Author  van Genderen MM Year  2009
Journal  Am J Hum Genet Volume  85
Issue  5 Pages  730-6
PubMed ID  19896109 Mgi Id 
Quick Links:
 
Quick Links:
 

Expression

Publication --> Expression annotations

 

Other

1 Bio Entities

Trail: Publication

0 Expression