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Q35209179-4567D7CB-A6D5-4879-A56F-5ACA77D761E7
Q35209179-4567D7CB-A6D5-4879-A56F-5ACA77D761E7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35209179-4567D7CB-A6D5-4879-A56F-5ACA77D761E7
Another evidence for a D47N mutation in GJA8 associated with autosomal dominant congenital cataract.
P2860
Q35209179-4567D7CB-A6D5-4879-A56F-5ACA77D761E7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35209179-4567D7CB-A6D5-4879-A56F-5ACA77D761E7
rank
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type
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Statement
wasDerivedFrom
36cc726a9c13bfede527db9fa9516fa1d5eb66d9
P2860
A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataract