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Q36605158-6000A231-1881-43B6-BB3A-A5EB7864EFB7
Q36605158-6000A231-1881-43B6-BB3A-A5EB7864EFB7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36605158-6000A231-1881-43B6-BB3A-A5EB7864EFB7
An MIP/AQP0 mutation with impaired trafficking and function underlies an autosomal dominant congenital lamellar cataract.
P2860
Q36605158-6000A231-1881-43B6-BB3A-A5EB7864EFB7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36605158-6000A231-1881-43B6-BB3A-A5EB7864EFB7
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wasDerivedFrom
28a2545dffda75fa72df84f26c7f905c15e1e3c7
P2860
Major intrinsic protein (MIP) polymorphism is associated with age-related cataract in Chinese.