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Q35891793-797F273B-2E3B-4DCB-88B6-A62F09DF9061
Q35891793-797F273B-2E3B-4DCB-88B6-A62F09DF9061
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35891793-797F273B-2E3B-4DCB-88B6-A62F09DF9061
Autosomal Recessive Bestrophinopathy Is Not Associated With the Loss of Bestrophin-1 Anion Channel Function in a Patient With a Novel BEST1 Mutation
P2860
Q35891793-797F273B-2E3B-4DCB-88B6-A62F09DF9061
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35891793-797F273B-2E3B-4DCB-88B6-A62F09DF9061
rank
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type
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wasDerivedFrom
ec7dff04f5287ff9dbe246a62ad61bc5c68bdb74
P2860
Biallelic mutation of BEST1 causes a distinct retinopathy in humans