Matches in Nanopublications for { ?s ?p "[Mutations in both the Kir6.2 and SUR1 genes are associated with persistent hyperinsulinemic hypoglycemia of infancy (PHHI), a disorder of pancreatic beta-cell function characterized by excess insulin secretion and hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP522694.RAdpv__kHWGBQwq7E5Q38csnb_8Hejwqa3Y9I0g9JylWg130_assertion description "[Mutations in both the Kir6.2 and SUR1 genes are associated with persistent hyperinsulinemic hypoglycemia of infancy (PHHI), a disorder of pancreatic beta-cell function characterized by excess insulin secretion and hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522694.RAdpv__kHWGBQwq7E5Q38csnb_8Hejwqa3Y9I0g9JylWg130_provenance.
- NP522801.RAT0vNbSi7Dmh27lH8YMha-x0UPo0MVigp5TCgJlN8bg0130_assertion description "[Mutations in both the Kir6.2 and SUR1 genes are associated with persistent hyperinsulinemic hypoglycemia of infancy (PHHI), a disorder of pancreatic beta-cell function characterized by excess insulin secretion and hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522801.RAT0vNbSi7Dmh27lH8YMha-x0UPo0MVigp5TCgJlN8bg0130_provenance.
- assertion description "[Mutations in both the Kir6.2 and SUR1 genes are associated with persistent hyperinsulinemic hypoglycemia of infancy (PHHI), a disorder of pancreatic beta-cell function characterized by excess insulin secretion and hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1398470.RAZp-xnL7Vi3djjunBO_7lAAwmbUS4KFhcVKP-cn9GB70130_assertion description "[Mutations in both the Kir6.2 and SUR1 genes are associated with persistent hyperinsulinemic hypoglycemia of infancy (PHHI), a disorder of pancreatic beta-cell function characterized by excess insulin secretion and hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1398470.RAZp-xnL7Vi3djjunBO_7lAAwmbUS4KFhcVKP-cn9GB70130_provenance.
- NP522710.RAyzdL0ALY_VBsIvLrz2RpXmXIZg2-DPkbkJ_ZwPQGx3c130_assertion description "[Mutations in both the Kir6.2 and SUR1 genes are associated with persistent hyperinsulinemic hypoglycemia of infancy (PHHI), a disorder of pancreatic beta-cell function characterized by excess insulin secretion and hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522710.RAyzdL0ALY_VBsIvLrz2RpXmXIZg2-DPkbkJ_ZwPQGx3c130_provenance.
- NP1398476.RAKp31GVkZ90f7aY8gi5CtZqiVum5AAUp6rN_Q_Y2Rsk4130_assertion description "[Mutations in both the Kir6.2 and SUR1 genes are associated with persistent hyperinsulinemic hypoglycemia of infancy (PHHI), a disorder of pancreatic beta-cell function characterized by excess insulin secretion and hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1398476.RAKp31GVkZ90f7aY8gi5CtZqiVum5AAUp6rN_Q_Y2Rsk4130_provenance.
- NP1398471.RAywcMwWoN0vf8HOI_6KOYMM678fQGuM8w2mZ20r2ld1s130_assertion description "[Mutations in both the Kir6.2 and SUR1 genes are associated with persistent hyperinsulinemic hypoglycemia of infancy (PHHI), a disorder of pancreatic beta-cell function characterized by excess insulin secretion and hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1398471.RAywcMwWoN0vf8HOI_6KOYMM678fQGuM8w2mZ20r2ld1s130_provenance.
- NP1398473.RA8U6U8B1X_yDvRniJbXcqnvYtHegSquGjWWnvEOdgzM0130_assertion description "[Mutations in both the Kir6.2 and SUR1 genes are associated with persistent hyperinsulinemic hypoglycemia of infancy (PHHI), a disorder of pancreatic beta-cell function characterized by excess insulin secretion and hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1398473.RA8U6U8B1X_yDvRniJbXcqnvYtHegSquGjWWnvEOdgzM0130_provenance.
- NP1398475.RA39yVTO3ggtb2sBPPZIGO1Lxisz94CEMaC4yk4LV5IUY130_assertion description "[Mutations in both the Kir6.2 and SUR1 genes are associated with persistent hyperinsulinemic hypoglycemia of infancy (PHHI), a disorder of pancreatic beta-cell function characterized by excess insulin secretion and hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1398475.RA39yVTO3ggtb2sBPPZIGO1Lxisz94CEMaC4yk4LV5IUY130_provenance.