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Q46409571-10405A99-2593-48D2-A5AD-610D9CBC94AB
Q46409571-10405A99-2593-48D2-A5AD-610D9CBC94AB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46409571-10405A99-2593-48D2-A5AD-610D9CBC94AB
A new familial form of a late-onset, persistent hyperinsulinemic hypoglycemia of infancy caused by a novel mutation in KCNJ11.
P2860
Q46409571-10405A99-2593-48D2-A5AD-610D9CBC94AB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46409571-10405A99-2593-48D2-A5AD-610D9CBC94AB
rank
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wasDerivedFrom
98904153fd49bcbd1083c74ce1c2e3602d953356
P2860
Relative expression of a dominant mutated ABCC8 allele determines the clinical manifestation of congenital hyperinsulinism.