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Q24297468-6A2B4307-B50B-42D0-8A39-22C8962C4348
Q24297468-6A2B4307-B50B-42D0-8A39-22C8962C4348
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24297468-6A2B4307-B50B-42D0-8A39-22C8962C4348
Monoallelic ABCC8 mutations are a common cause of diazoxide-unresponsive diffuse form of congenital hyperinsulinism
P2860
Q24297468-6A2B4307-B50B-42D0-8A39-22C8962C4348
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24297468-6A2B4307-B50B-42D0-8A39-22C8962C4348
rank
NormalRank
type
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Statement
wasDerivedFrom
ddc00f45d9be22e6cd7be45e62ab8499bfc7cce5
P2860
Congenital hyperinsulinism associated ABCC8 mutations that cause defective trafficking of ATP-sensitive K+ channels: identification and rescue