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Q57920463-58BCB137-7C7F-43D8-9BA4-F732D3529167
Q57920463-58BCB137-7C7F-43D8-9BA4-F732D3529167
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Statement
http://www.wikidata.org/entity/statement/Q57920463-58BCB137-7C7F-43D8-9BA4-F732D3529167
Heterozygous ABCC8 mutations are a cause of MODY
P2860
Q57920463-58BCB137-7C7F-43D8-9BA4-F732D3529167
BestRank
Statement
http://www.wikidata.org/entity/statement/Q57920463-58BCB137-7C7F-43D8-9BA4-F732D3529167
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wasDerivedFrom
832a06b5278624518b22b02ea9bf80cb7460ab28
P2860
A rare mutation in ABCC8/SUR1 leading to altered ATP-sensitive K+ channel activity and beta-cell glucose sensing is associated with type 2 diabetes in adults.