Publication not explained
This publication has not yet been explained in plain language by the author(s). However, you can still read the publication.
If you are one of the authors, claim this publication so you can create a plain language summary to help more people find, understand and use it.
Featured Image
Read the Original
This page is a summary of: Abrogation of HMX1 Function Causes Rare Oculoauricular Syndrome Associated With Congenital Cataract, Anterior Segment Dysgenesis, and Retinal Dystrophy, Investigative Ophthalmology & Visual Science, January 2015, Association for Research in Vision and Ophthalmology (ARVO),
DOI: 10.1167/iovs.14-15861.
You can read the full text:
Contributors
The following have contributed to this page