:FBXW7

Yu Wang1, Xiaoping Ma2, Hua Li2

  • 1College of Clinical Medicine, Ningxia Medical University, Yinchuan, China.

Frontiers in genetics
|October 4, 2024
PubMed
概括

这项研究报告说,儿童患有罕见的神经发育障碍,由FBXW7基因的新突变引起. 这些发现强调了遗传性疾病.

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