Title : Genotype and phenotype correlations in 417 children with congenital hyperinsulinism.

Pub. Date : 2013 Feb

PMID : 23275527






1 Functional Relationships(s)
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1 METHODS: Mutation analysis was carried out for the ATP-sensitive potassium (KATP) channel genes (ABCC8 and KCNJ11), GLUD1, and GCK with supplemental screening of rarer genes, HADH, UCP2, HNF4A, HNF1A, and SLC16A1. Adenosine Triphosphate ATP binding cassette subfamily C member 8 Homo sapiens