案例报告:INSR中错误变异的功能性表征与低血糖症相关

Herodes Guzman1,2, Lauren M Mitteer1, Pan Chen1

  • 1Division of Endocrinology and Diabetes, Children's Hospital of Philadelphia, Philadelphia, PA, United States.

Frontiers in pediatrics
|November 1, 2024
PubMed
概括

胰岛素受体 (INSR) 基因中的遗传变异导致儿童患持续性低血糖症. 这一发现强调了INSR基因缺陷是低血糖症的原因,影响了治疗策略.

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