Associated Papers
Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts.
Irum B et al.
Plos One, 2016
Investigation of invariant serine/threonine residues in mevalonate kinase. Tests of the functional significance of a proposed substrate binding motif and a site implicated in human inherited disease.
Cho YK et al.
The Journal of Biological Chemistry, 2001
Select a paper to view details