首页> Journal of pediatric endocrinology & metabolism: JPEM> Glycogen storage disease type IIIa presenting as non-ketotic hypoglycemia: use of a newly approved commercially available mutation analysis to non-invasively confirm the diagnosis.

Glycogen storage disease type IIIa presenting as non-ketotic hypoglycemia: use of a newly approved commercially available mutation analysis to non-invasively confirm the diagnosis.

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第一作者： Seigel J

作者： Seigel J ^[1] ; Weinstein DA ; Hillman R ; Colbert B ; Matthews B ; Bachrach B

作者单位： Division of Pediatric Endocrinology, University of Missouri-Columbia School of Medicine, Columbia, MO 65212, USA. ^[1]

关键词 DNA Mutational Analysis Diagnosis Differential Glycogen Storage Disease Type III DNA突变分析诊断鉴别糖原累积病Ⅲ型低血糖症婴儿试剂盒

发布时间 2013-11-20

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Journal of pediatric endocrinology & metabolism

2008年21卷6期

587-590页

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Journal of pediatric endocrinology & metabolism

2008年21卷6期

587-590页

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Glycogen storage disease type IIIa presenting as non-ketotic hypoglycemia: use of a newly approved commercially available mutation analysis to non-invasively confirm the diagnosis.

Journal of pediatric endocrinology & metabolism

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Journal of pediatric endocrinology & metabolism

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Glycogen storage disease type IIIa presenting as non-ketotic hypoglycemia: use of a newly approved commercially available mutation analysis to non-invasively confirm the diagnosis.

Journal of pediatric endocrinology & metabolism

相似文献

同项目论文

Journal of pediatric endocrinology & metabolism

相关期刊

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