Matches in Nanopublications for { ?s ?p "[The second most common form of congenital hyperinsulinism, the hyperinsulinism/hyperammonemia syndrome (HI/HA), is associated with dominantly expressed missense mutations of the mitochondrial matrix enzyme, glutamate dehydrogenase (GDH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP887543.RAeUirQ9d5_JDDx0PTJBU4YUVySgx7qV46qoBr2o0o91o130_assertion description "[The second most common form of congenital hyperinsulinism, the hyperinsulinism/hyperammonemia syndrome (HI/HA), is associated with dominantly expressed missense mutations of the mitochondrial matrix enzyme, glutamate dehydrogenase (GDH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887543.RAeUirQ9d5_JDDx0PTJBU4YUVySgx7qV46qoBr2o0o91o130_provenance.
- NP312496.RAdw47y7kHK7n22BBiRa6tDvYztT3lHx9N5UcqJ-vB97Y130_assertion description "[The second most common form of congenital hyperinsulinism, the hyperinsulinism/hyperammonemia syndrome (HI/HA), is associated with dominantly expressed missense mutations of the mitochondrial matrix enzyme, glutamate dehydrogenase (GDH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP312496.RAdw47y7kHK7n22BBiRa6tDvYztT3lHx9N5UcqJ-vB97Y130_provenance.
- NP160606.RAiJDmADGr028MAobhKyBis6yUSPZ-lv_0jQiT_YRqa5s130_assertion description "[The second most common form of congenital hyperinsulinism, the hyperinsulinism/hyperammonemia syndrome (HI/HA), is associated with dominantly expressed missense mutations of the mitochondrial matrix enzyme, glutamate dehydrogenase (GDH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP160606.RAiJDmADGr028MAobhKyBis6yUSPZ-lv_0jQiT_YRqa5s130_provenance.
- NP723047.RAiJuuXROs51WQ0K0_YRWOZW4Ivlwi_funsuuGLWpvswc130_assertion description "[The second most common form of congenital hyperinsulinism, the hyperinsulinism/hyperammonemia syndrome (HI/HA), is associated with dominantly expressed missense mutations of the mitochondrial matrix enzyme, glutamate dehydrogenase (GDH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723047.RAiJuuXROs51WQ0K0_YRWOZW4Ivlwi_funsuuGLWpvswc130_provenance.
- NP656865.RAnKmOg8v0SeEcVRFcXKeN12eo8nn7fuKRsX8j5I9DxXw130_assertion description "[The second most common form of congenital hyperinsulinism, the hyperinsulinism/hyperammonemia syndrome (HI/HA), is associated with dominantly expressed missense mutations of the mitochondrial matrix enzyme, glutamate dehydrogenase (GDH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP656865.RAnKmOg8v0SeEcVRFcXKeN12eo8nn7fuKRsX8j5I9DxXw130_provenance.
- NP328915.RA1mgx3JAMDQp8cjO9h8yWKuKhOIFf7_FrsY0ZPIGeYCY130_assertion description "[The second most common form of congenital hyperinsulinism, the hyperinsulinism/hyperammonemia syndrome (HI/HA), is associated with dominantly expressed missense mutations of the mitochondrial matrix enzyme, glutamate dehydrogenase (GDH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP328915.RA1mgx3JAMDQp8cjO9h8yWKuKhOIFf7_FrsY0ZPIGeYCY130_provenance.
- NP838015.RA3O5ZdfGpPx-4urJlZUhC2JTqLr_7CGop7SHLCrw43-8130_assertion description "[The second most common form of congenital hyperinsulinism, the hyperinsulinism/hyperammonemia syndrome (HI/HA), is associated with dominantly expressed missense mutations of the mitochondrial matrix enzyme, glutamate dehydrogenase (GDH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP838015.RA3O5ZdfGpPx-4urJlZUhC2JTqLr_7CGop7SHLCrw43-8130_provenance.
- NP752895.RAE0nktUgqucP5myFUhLwaM-CzbORQOHxcpsIt3cNzC8Y130_assertion description "[The second most common form of congenital hyperinsulinism, the hyperinsulinism/hyperammonemia syndrome (HI/HA), is associated with dominantly expressed missense mutations of the mitochondrial matrix enzyme, glutamate dehydrogenase (GDH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP752895.RAE0nktUgqucP5myFUhLwaM-CzbORQOHxcpsIt3cNzC8Y130_provenance.