CTNNB1基因变异致伴有痉挛性双瘫和视觉缺陷的神经发育障碍5例报告并文献复习

庞可心, 王培, 朱敏, 陆芬, 汤健, 张丽

Neurodevelopmental disorder with spastic diplegia and visual defects by CTNNB1 gene mutation: a report of 5 Chinese cases with literature review

PANG Kexin, WANG Pei, ZHU Min, LU Fen, TANG Jian, ZHANG Li

临床儿科杂志 . 2022, (8): 616 -622 . DOI: 10.12372/jcp.2022.21e1421