1 – 4 of 4
- show: 5
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2016
-
Mark
Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation Sequencing.
(
- Contribution to journal › Article
- 2012
-
Mark
Mutations in RPGR and RP2 Account for 15% of Males with Simplex Retinal Degenerative Disease
(
- Contribution to journal › Article
- 2009
-
Mark
Mutations in a BTB-Kelch Protein, KLHL7, Cause Autosomal-Dominant Retinitis Pigmentosa
(
- Contribution to journal › Article
- 2006
-
Mark
Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degeneration
(
- Contribution to journal › Article