Proline

crystallin gamma D ; Homo sapiens







2 Article(s)
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Title
Pub. Year
#Total Relationships
1 21552497 A recurrent mutation in CRYGD is associated with autosomal dominant congenital coralliform cataract in two unrelated Chinese families. 2011 Apr 28 1
2 15041957 A missense mutation in the gammaD crystallin gene (CRYGD) associated with autosomal dominant "coral-like" cataract linked to chromosome 2q. 2004 Mar 17 3