A novel missense mutation in the gene for gap-junction protein α3 (GJA3) associated with autosomal dominant “nuclear punctate” cataracts linked to chromosome 13q

Authors

Thomas M. Bennett, Washington University School of Medicine in St. LouisFollow
Donna S. Mackay, Washington University School of Medicine in St. Louis
Harry L.S. Knopf, 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

376-382

Document Type

Open Access Publication

Rights and Permissions

Bennett, T. M., Mackay, D. S., Knopf, H. L. S., & Shiels, A. (2004). A novel missense mutation in the gene for gap-junction protein α3 (GJA3) associated with autosomal dominant "nuclear punctate" cataracts linked to chromosome 13q. Molecular Vision, 10, 376-382. http://www.molvis.org/molvis/v10/a47/

Recommended Citation

Bennett, Thomas M.; Mackay, Donna S.; Knopf, Harry L.S.; and Shiels, Alan, "A novel missense mutation in the gene for gap-junction protein α3 (GJA3) associated with autosomal dominant “nuclear punctate” cataracts linked to chromosome 13q." Molecular Vision. 10, 376-382. (2004).
https://digitalcommons.wustl.edu/open_access_pubs/1806