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1750-1172-9-26
1750-1172-9-26
https://scigraph.springernature.com/pub.10.1186/1750-1172-9-26
Novel and recurrent PITX3 mutations in Belgian families with autosomal dominant congenital cataract and anterior segment dysgenesis have similar phenotypic and functional characteristics.
P2888
Q37608059-57F2D1C7-36D0-43D2-98B2-0ABD0DB06069
P2888
1750-1172-9-26
https://scigraph.springernature.com/pub.10.1186/1750-1172-9-26