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Volumn 94, Issue 2, 2008, Pages 268-269

Gene duplications resulting in over expression of glucokinase are not a common cause of hypoglycaemia of infancy in humans

Author keywords

[No Author keywords available]

Indexed keywords

GLUCOKINASE;

EID: 43449087616     PISSN: 10967192     EISSN: 10967206     Source Type: Journal    
DOI: 10.1016/j.ymgme.2008.01.008     Document Type: Letter
Times cited : (4)

References (11)
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  • 3
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    • Large genomic rearrangements in the hepatocyte nuclear factor-1beta (TCF2) gene are the most frequent cause of maturity-onset diabetes of the young type 5
    • Bellanne-Chantelot C., Clauin S., Chauveau D., Collin P., Daumont M., Douillard C., et al. Large genomic rearrangements in the hepatocyte nuclear factor-1beta (TCF2) gene are the most frequent cause of maturity-onset diabetes of the young type 5. Diabetes 54 11 (2005) 3126-3132
    • (2005) Diabetes , vol.54 , Issue.11 , pp. 3126-3132
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  • 4
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    • Partial and whole gene deletion mutations of the GCK and HNF1A genes in maturity-onset diabetes of the young
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  • 5
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    • Mechanisms of disease: advances in diagnosis and treatment of hyperinsulinism in neonates
    • De Leon D.D., and Stanley C.A. Mechanisms of disease: advances in diagnosis and treatment of hyperinsulinism in neonates. Nat. Clin. Pract. Endocrinol. Metab. 3 1 (2007) 57-68
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    • De Leon, D.D.1    Stanley, C.A.2
  • 6
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    • Gloyn A.L. Glucokinase (GCK) mutations in hyper- and hypoglycemia: maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemia of infancy. Hum. Mutat. 22 5 (2003) 353-362
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.