Associated Papers
Pleiotropic effect of a novel mutation in GCNT2 causing congenital cataract and a rare adult i blood group phenotype.
Cheong SS et al.
Human Genome Variation, 2017
Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts.
Irum B et al.
Plos One, 2016
A nonsense mutation in the glucosaminyl (N-acetyl) transferase 2 gene (GCNT2): association with autosomal recessive congenital cataracts.
Pras E et al.
Investigative Ophthalmology & Visual Science, 2004
A novel I-branching beta-1,6-N-acetylglucosaminyltransferase involved in human blood group I antigen expression.
Inaba N et al.
Blood, 2003
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