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Detection of KCNJ11 gene mutations in a family with neonatal diabetes mellitus: Implications for therapeutic management of family members with long-standing disease

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作者： Abbasi,F. ^[1] ; Saba,S. ; Ebrahim-Habibi,A. ; Sayahpour,F.A. ; Amiri,P. ; Larijani,B. ; Amoli,M.M.

作者单位： Endocrinology and Metabolism Research Center, Tehran University of Medical Sciences, Dr Shariati ^[1]

关键词 Clinical-genetics Diabetes-mellitus Genetic-polymorphism Glibenclamide Insulin Neonatal-disorders Sulfonylureas

发布时间 2013-11-20

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Molecular diagnosis & therapy

2012年16卷2期

109-114页

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Molecular diagnosis & therapy

2012年16卷2期

109-114页

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Detection of KCNJ11 gene mutations in a family with neonatal diabetes mellitus: Implications for therapeutic management of family members with long-standing disease

Molecular diagnosis & therapy

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Molecular diagnosis & therapy

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Detection of KCNJ11 gene mutations in a family with neonatal diabetes mellitus: Implications for therapeutic management of family members with long-standing disease

Molecular diagnosis & therapy

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Molecular diagnosis & therapy

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