案例报告:在一个发育迟缓和身材矮小的中国男孩身上发现了一种新的PRR12变异

Zhengxia Liu1, Shuxia Ding2, Guangwei Xu3

  • 1Department of Neurology, Women and Children's Hospital Affiliated to Ningbo University, Ningbo, Zhejiang, China.

PubMed
概括

这项研究详细介绍了一名智力障碍和多动症的中国男孩的新型Proline Rich 12 (PRR12) 基因变异. 这些发现扩大了对PRR12变体和神经发育障碍的理解.

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