A missense mutation in the γD crystallin gene (CRYGD) associated with autosomal dominant "coral-like" cataract linked to chromosome 2q

Authors

Donna S. Mackay, Washington University School of Medicine in St. Louis
Usha P. Andley, Washington University School of Medicine in St. Louis
Alan Shiels, Washington University School of Medicine in St. Louis

Journal

Molecular Vision

Publication Date

2004

Volume

10

Inclusive Pages

155-162

Document Type

Open Access Publication

Rights and Permissions

Mackay, D. S., Andley, U. P., & Shiels, A. (2004). A missense mutation in the γD crystallin gene (CRYGD) associated with autosomal dominant "coral-like" cataract linked to chromosome 2q. Molecular Vision, 10, 155-162. http://www.molvis.org/molvis/v10/a21/

Recommended Citation

Mackay, Donna S.; Andley, Usha P.; and Shiels, Alan, "A missense mutation in the γD crystallin gene (CRYGD) associated with autosomal dominant "coral-like" cataract linked to chromosome 2q." Molecular Vision. 10, 155-162. (2004).
https://digitalcommons.wustl.edu/open_access_pubs/1805