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Q36766108-B1168830-44B1-427B-9A19-35E9439D7A2A
Q36766108-B1168830-44B1-427B-9A19-35E9439D7A2A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36766108-B1168830-44B1-427B-9A19-35E9439D7A2A
A novel connexin 50 gene (gap junction protein, alpha 8) mutation associated with congenital nuclear and zonular pulverulent cataract.
P921
Q36766108-B1168830-44B1-427B-9A19-35E9439D7A2A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36766108-B1168830-44B1-427B-9A19-35E9439D7A2A
rank
NormalRank
type
BestRank
Statement
P921
birth defect