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Q38606557-0F9520A0-3468-4EC5-AF7E-B2FC781DD0DE
Q38606557-0F9520A0-3468-4EC5-AF7E-B2FC781DD0DE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38606557-0F9520A0-3468-4EC5-AF7E-B2FC781DD0DE
Clinical and genetic findings in a family with NMNAT1-associated Leber congenital amaurosis: case report and review of the literature.
P2860
Q38606557-0F9520A0-3468-4EC5-AF7E-B2FC781DD0DE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38606557-0F9520A0-3468-4EC5-AF7E-B2FC781DD0DE
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Statement
wasDerivedFrom
6a00ad86c17f5d3b57a40ac88f9f03482d6bf8bb
P2860
The phenotype of Leber congenital amaurosis in patients with AIPL1 mutations.