The WDR36 Gene on Chromosome 5q22.1 Is Not Responsible for POAG in a Large Family That Maps to This Region

Elena Morris(Oregon Health & Science University), Mary K. Wirtz(Legacy Health), M. Sarfarazi(UConn Health), Reneé Sykes(Oregon Health & Science University), J. R. Samples(Oregon Health & Science University), P. L. Kramer(Oregon Health & Science University), Sharareh Monemi(UConn Health)
Investigative Ophthalmology & Visual Science
May 1, 2006
Cited by 0

Related Papers

Consensus recommendations for trabecular meshwork cell isolation, characterization and culture
|Experimental Eye Research|2018|345
In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome: Figure 1
|Journal of Medical Genetics|2003|281
Autosomal Dominant Cerulean Cataract Is Associated with a Chain Termination Mutation in the Human  -Crystallin Gene CRYBB2
|Human Molecular Genetics|1997|241
Mapping a gene for adult-onset primary open-angle glaucoma to chromosome 3q.
|PubMed|1997|212
GLC1F, A New Primary Open-angle Glaucoma Locus, Maps to 7q35-q36
|Archives of Ophthalmology|1999|182