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Q37608059-F3A7CD36-3BBD-4EC1-B377-197DDE4CD012
Q37608059-F3A7CD36-3BBD-4EC1-B377-197DDE4CD012
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37608059-F3A7CD36-3BBD-4EC1-B377-197DDE4CD012
Novel and recurrent PITX3 mutations in Belgian families with autosomal dominant congenital cataract and anterior segment dysgenesis have similar phenotypic and functional characteristics.
P2093
Q37608059-F3A7CD36-3BBD-4EC1-B377-197DDE4CD012
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37608059-F3A7CD36-3BBD-4EC1-B377-197DDE4CD012
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
fe4fda9c5b3be039ddaa950da032224e7e8b1e2a
P1545
1
http://www.w3.org/2001/XMLSchema#string
P2093
Hannah Verdin
http://www.w3.org/2001/XMLSchema#string