Fingerprint
Dive into the research topics of 'De novo mutations in the CRX homeobox gene associated with leber congenital amaurosis'. Together they form a unique fingerprint.- Sort by
- Weight
- Alphabetically
De novo mutations in the CRX homeobox gene associated with leber congenital amaurosis
Carol L. Freund, Qing Liang Wang, Shiming Chen, Brenda L. Muskat, Carmella D. Wiles, Val C. Sheffield, Samuel G. Jacobson, Roderick R. McLnnes, Donald J. Zack, Edwin M. Stone
- Department of Ophthalmology and Visual Sciences
- Roy and Diana Vagelos Division of Biology & Biomedical Sciences (DBBS)
- Institute of Clinical and Translational Sciences (ICTS)
- Center of Regenerative Medicine
- DBBS - Neurosciences
- DBBS - Developmental, Regenerative and Stem Cell Biology
- DBBS - Molecular Genetics and Genomics
Research output: Contribution to journal › Letter › peer-review
263
Scopus
citations