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Q37058489-150BAA2B-B6A8-48DE-922B-841DD269B81B
Q37058489-150BAA2B-B6A8-48DE-922B-841DD269B81B
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http://www.wikidata.org/entity/statement/Q37058489-150BAA2B-B6A8-48DE-922B-841DD269B81B
Rare FOXC1 variants in congenital glaucoma: identification of translation regulatory sequences.
P2860
Q37058489-150BAA2B-B6A8-48DE-922B-841DD269B81B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37058489-150BAA2B-B6A8-48DE-922B-841DD269B81B
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wasDerivedFrom
9100ed5f3f966b3f08f723802582074b5f5c0df4
P2860
MYOC gene mutations in Spanish patients with autosomal dominant primary open-angle glaucoma: a founder effect in southeast Spain.