Matches in Nanopublications for { ?s ?p "[We report a girl with congenital hyperinsulinism due to novel homozygous mutation (c.2041-25 G>A; aberrant splicing mutation) in the ABCC8 gene encoding SUR1 and during somatostatin analog (octreotide) discontinuation developed by nonhypoglycemic seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP348647.RATsb7Wo0emZ4SvbEQ3j_ofJwSB7gHas5s94E_qzsx5Gk130_assertion description "[We report a girl with congenital hyperinsulinism due to novel homozygous mutation (c.2041-25 G>A; aberrant splicing mutation) in the ABCC8 gene encoding SUR1 and during somatostatin analog (octreotide) discontinuation developed by nonhypoglycemic seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP348647.RATsb7Wo0emZ4SvbEQ3j_ofJwSB7gHas5s94E_qzsx5Gk130_provenance.
- NP698543.RAd5cbLZZkHrOrUpezd1Dl5Y5S3zFiM5vi92vG4dHXQQ8130_assertion description "[We report a girl with congenital hyperinsulinism due to novel homozygous mutation (c.2041-25 G>A; aberrant splicing mutation) in the ABCC8 gene encoding SUR1 and during somatostatin analog (octreotide) discontinuation developed by nonhypoglycemic seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP698543.RAd5cbLZZkHrOrUpezd1Dl5Y5S3zFiM5vi92vG4dHXQQ8130_provenance.
- NP575368.RAMv7e0ckd1DJg9sBJTGnU48fGwv-jL4wPAwk98dUXBI4130_assertion description "[We report a girl with congenital hyperinsulinism due to novel homozygous mutation (c.2041-25 G>A; aberrant splicing mutation) in the ABCC8 gene encoding SUR1 and during somatostatin analog (octreotide) discontinuation developed by nonhypoglycemic seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP575368.RAMv7e0ckd1DJg9sBJTGnU48fGwv-jL4wPAwk98dUXBI4130_provenance.