Associated Papers
Molecular genetics of congenital nuclear cataract.
Deng H et al.
European Journal of Medical Genetics, 2014
Structural and aggregation behavior of the human γD-crystallin mutant E107A, associated with congenital nuclear cataract.
Vendra VP et al.
Molecular Vision, 2010
Dense nuclear cataract caused by the gammaB-crystallin S11R point mutation.
Li L et al.
Investigative Ophthalmology & Visual Science, 2008
Interdomain side-chain interactions in human gammaD crystallin influencing folding and stability.
Flaugh SL et al.
Protein Science : a Publication of the Protein Society, 2005
Genetic disorders involving molecular-chaperone genes: a perspective.
Macario AJ et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2005
Gamma-D crystallin gene (CRYGD) mutation causes autosomal dominant congenital cerulean cataracts.
Nandrot E et al.
Journal of Medical Genetics, 2003
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