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HUMU.21386
HUMU.21386
http://dx.doi.org/10.1002/HUMU.21386
A novel CRYGD mutation (p.Trp43Arg) causing autosomal dominant congenital cataract in a Chinese family.
P356
Q34561463-358B8749-074E-43BC-8B42-C3F0959B9B28
P356
HUMU.21386
http://dx.doi.org/10.1002/HUMU.21386