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Q24624430-37A9A0C3-4FC7-4C1C-8C0D-0E30D85C29A2
Q24624430-37A9A0C3-4FC7-4C1C-8C0D-0E30D85C29A2
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http://www.wikidata.org/entity/statement/Q24624430-37A9A0C3-4FC7-4C1C-8C0D-0E30D85C29A2
Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration
P2860
Q24624430-37A9A0C3-4FC7-4C1C-8C0D-0E30D85C29A2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24624430-37A9A0C3-4FC7-4C1C-8C0D-0E30D85C29A2
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9d43ffbe214158894309090caf9cba139698fa48
P2860
IQCB1 mutations in patients with leber congenital amaurosis.