Fingerprint
Dive into the research topics of 'Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA'. Together they form a unique fingerprint.- Sort by
- Weight
- Alphabetically
Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA
Michael Litt, Patricia Kramer, Dante M. LaMorticella, William Murphey, Everett W. Lovrien, Richard G. Weleber
Research output: Contribution to journal › Article › peer-review
425
Scopus
citations