Matches in Nanopublications for { ?s ?p "[Mutations in SUR have been identified in individuals affected with familial persistent hyper-insulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder of glucose metabolism which is linked to chromosome 11p15.1 and characterized by unregulated secretion of insulin and profound hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP517070.RADY0p_e-V7fSYgJaEFp-y_JsSTep6zuMMC3iI-EHvsZM130_assertion description "[Mutations in SUR have been identified in individuals affected with familial persistent hyper-insulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder of glucose metabolism which is linked to chromosome 11p15.1 and characterized by unregulated secretion of insulin and profound hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP517070.RADY0p_e-V7fSYgJaEFp-y_JsSTep6zuMMC3iI-EHvsZM130_provenance.
- NP755806.RAUtmCVTekftA8AVF9RRfWwJhrDP5m1N7LXEygCEI1_bc130_assertion description "[Mutations in SUR have been identified in individuals affected with familial persistent hyper-insulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder of glucose metabolism which is linked to chromosome 11p15.1 and characterized by unregulated secretion of insulin and profound hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755806.RAUtmCVTekftA8AVF9RRfWwJhrDP5m1N7LXEygCEI1_bc130_provenance.
- NP822317.RAldYAL-oaltDanHq6DWGUu1TmNAcOtvzGaXcYx_dKzOQ130_assertion description "[Mutations in SUR have been identified in individuals affected with familial persistent hyper-insulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder of glucose metabolism which is linked to chromosome 11p15.1 and characterized by unregulated secretion of insulin and profound hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP822317.RAldYAL-oaltDanHq6DWGUu1TmNAcOtvzGaXcYx_dKzOQ130_provenance.
- NP657721.RALpjAqDoptF23msiUQbiTTm1XY_FLdnhh-mnb36SQUK0130_assertion description "[Mutations in SUR have been identified in individuals affected with familial persistent hyper-insulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder of glucose metabolism which is linked to chromosome 11p15.1 and characterized by unregulated secretion of insulin and profound hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP657721.RALpjAqDoptF23msiUQbiTTm1XY_FLdnhh-mnb36SQUK0130_provenance.
- NP512842.RAb9AVEu1v7QrXrHHiCeC6BTzZXYEficKeq5jecdQHXtM130_assertion description "[Mutations in SUR have been identified in individuals affected with familial persistent hyper-insulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder of glucose metabolism which is linked to chromosome 11p15.1 and characterized by unregulated secretion of insulin and profound hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP512842.RAb9AVEu1v7QrXrHHiCeC6BTzZXYEficKeq5jecdQHXtM130_provenance.
- NP1008497.RA5ClBcNMyJheKAjStqzPECNW_7MlvV5YmEb4e3zdUbPw130_assertion description "[Mutations in SUR have been identified in individuals affected with familial persistent hyper-insulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder of glucose metabolism which is linked to chromosome 11p15.1 and characterized by unregulated secretion of insulin and profound hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1008497.RA5ClBcNMyJheKAjStqzPECNW_7MlvV5YmEb4e3zdUbPw130_provenance.
- NP1362724.RAQ2aVTeQ-V3Bl_NmgNiYxFkGRwd-L9ieKNt1Nlhq4roQ130_assertion description "[Mutations in SUR have been identified in individuals affected with familial persistent hyper-insulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder of glucose metabolism which is linked to chromosome 11p15.1 and characterized by unregulated secretion of insulin and profound hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1362724.RAQ2aVTeQ-V3Bl_NmgNiYxFkGRwd-L9ieKNt1Nlhq4roQ130_provenance.
- NP1362723.RALrj-_zLO9lNJXrPIIx20f_ERMqWOwFYgZkgzAWzyITo130_assertion description "[Mutations in SUR have been identified in individuals affected with familial persistent hyper-insulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder of glucose metabolism which is linked to chromosome 11p15.1 and characterized by unregulated secretion of insulin and profound hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1362723.RALrj-_zLO9lNJXrPIIx20f_ERMqWOwFYgZkgzAWzyITo130_provenance.