Citations for
1BGIS, GCNT2
An Alu repeat-mediated genomic GCNT2 deletion underlies congenital cataracts and adult i blood group.
Borck G, Kakar N, Hoch J, Friedrich K, Freudenberg J, Nürnberg G, Yilmaz R, Daud S, Baloch DM, Nürnberg P, Oldenburg J, Ahmad J, Kubisch C.
Hum Genet 131(2):209-16. doi: 10.1007/s00439-011-1062-1. Epub 2011 Jul 15. 2012
2BGIS, GCNT2
A nonsense mutation in the glucosaminyl (N-acetyl) transferase 2 gene (GCNT2): association with autosomal recessive congenital cataracts.
Pras E, Raz J, Yahalom V, Frydman M, Garzozi HJ, Pras E, Hejtmancik JF.
Invest Ophthalmol Vis Sci 45(6):1940-5. 2004