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Q37452617-1E0D3450-CEFE-48E1-B485-935792F63446
Q37452617-1E0D3450-CEFE-48E1-B485-935792F63446
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Statement
http://www.wikidata.org/entity/statement/Q37452617-1E0D3450-CEFE-48E1-B485-935792F63446
A novel VSX1 mutation identified in an individual with keratoconus in India
P2860
Q37452617-1E0D3450-CEFE-48E1-B485-935792F63446
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37452617-1E0D3450-CEFE-48E1-B485-935792F63446
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wasDerivedFrom
8c7327e3df94e8b3ce4f2ae7d8132abb6c75af49
P2860
The phenotype of Leber congenital amaurosis in patients with AIPL1 mutations.