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Q28270488-7856C6EA-B5BE-4329-A45F-F1F2E9DF5932
Q28270488-7856C6EA-B5BE-4329-A45F-F1F2E9DF5932
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Statement
http://www.wikidata.org/entity/statement/Q28270488-7856C6EA-B5BE-4329-A45F-F1F2E9DF5932
Comprehensive genotyping reveals RPE65 as the most frequently mutated gene in Leber congenital amaurosis in Denmark
P2860
Q28270488-7856C6EA-B5BE-4329-A45F-F1F2E9DF5932
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28270488-7856C6EA-B5BE-4329-A45F-F1F2E9DF5932
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Statement
wasDerivedFrom
8f1cc90f20d5c49e659ac2e3a4fa5939fd25bd5c
P2860
Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis