Hereditary Transthyretin Amyloidosis in Eight Chinese Families

por Meng, Ling-Chao, Lyu, He, Zhang, Wei, Liu, Jing, Wang, Zhao-Xia, Yuan, Yun
Publicado 2015

A de novo variant of POLR3B causes demyelinating Charcot-Marie-Tooth disease in a Chinese patient: a case report

por Xue, Yan-Yan, Cheng, Hao-Ling, Dong, Hai-Lin, Yin, Hou-Min, Yuan, Yun, Meng, Ling-Chao, Wu, Zhi-Ying, Yu, Hao
Publicado 2021

The GGC repeat expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy type 3

por Yu, Jiaxi, Deng, Jianwen, Guo, Xueyu, Shan, Jingli, Luan, Xinghua, Cao, Li, Zhao, Juan, Yu, Meng, Zhang, Wei, Lv, He, Xie, Zhiying, Meng, LingChao, Zheng, Yiming, Zhao, Yawen, Gang, Qiang, Wang, Qingqing, Liu, Jing, Zhu, Min, Zhou, Binbin, Li, Pidong, Liu, Yinzhe, Wang, Yang, Yan, Chuanzhu, Hong, Daojun, Yuan, Yun, Wang, Zhaoxia
Publicado 2021