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Q37608059-D91686F1-4B90-471F-962F-AA988C139B63
Q37608059-D91686F1-4B90-471F-962F-AA988C139B63
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http://www.wikidata.org/entity/statement/Q37608059-D91686F1-4B90-471F-962F-AA988C139B63
Novel and recurrent PITX3 mutations in Belgian families with autosomal dominant congenital cataract and anterior segment dysgenesis have similar phenotypic and functional characteristics.
P2860
Q37608059-D91686F1-4B90-471F-962F-AA988C139B63
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37608059-D91686F1-4B90-471F-962F-AA988C139B63
rank
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type
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Statement
wasDerivedFrom
b1f16ef685563f782b7f4679e0f28a61fffb1e5e
P2860
Missense mutations in the most ancient residues of the PAX6 paired domain underlie a spectrum of human congenital eye malformations.