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Q37346452-58B26B87-C393-4EA7-A4A0-3E0A17D55B38
Q37346452-58B26B87-C393-4EA7-A4A0-3E0A17D55B38
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37346452-58B26B87-C393-4EA7-A4A0-3E0A17D55B38
The GJA8 allele encoding CX50I247M is a rare polymorphism, not a cataract-causing mutation.
P2860
Q37346452-58B26B87-C393-4EA7-A4A0-3E0A17D55B38
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37346452-58B26B87-C393-4EA7-A4A0-3E0A17D55B38
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Statement
wasDerivedFrom
70eccf0a0c0f5f369d451e432d40e4e329413bd5
P2860
A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataract