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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2009 | 1 |
2011 | 1 |
2016 | 1 |
2024 | 0 |
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Opposite clinical phenotypes of glucokinase disease: Description of a novel activating mutation and contiguous inactivating mutations in human glucokinase (GCK) gene.
Mol Endocrinol. 2009 Dec;23(12):1983-9. doi: 10.1210/me.2009-0094. Epub 2009 Nov 2.
Mol Endocrinol. 2009.
PMID: 19884385
Free PMC article.
Mutational analysis of allosteric activation and inhibition of glucokinase.
Zelent B, Odili S, Buettger C, Zelent DK, Chen P, Fenner D, Bass J, Stanley C, Laberge M, Vanderkooi JM, Sarabu R, Grimsby J, Matschinsky FM.
Zelent B, et al.
Biochem J. 2011 Dec 1;440(2):203-15. doi: 10.1042/BJ20110440.
Biochem J. 2011.
PMID: 21831042
Free PMC article.
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Clinical and genetic characterization of congenital hyperinsulinism in Spain.
Martínez R, Fernández-Ramos C, Vela A, Velayos T, Aguayo A, Urrutia I, Rica I, Castaño L; Spanish Congenital Hyperinsulinism Group.
Martínez R, et al.
Eur J Endocrinol. 2016 Jun;174(6):717-26. doi: 10.1530/EJE-16-0027.
Eur J Endocrinol. 2016.
PMID: 27188453
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