The complete mitochondrial genome sequence of Ptyas mucosus

por Zhou, Bo, Ding, Changhong, Duan, Yubao, Hui, Guo
Publicado 2016

Multisource Deep Transfer Learning Based on Balanced Distribution Adaptation

por Gao, Peng, Li, Jingmei, Zhao, Guodong, Ding, Changhong
Publicado 2022

Sequencing and analysis of mitochondrial genome of Elaphe carinata (Reptilia, Squamata, Colubridae)

por Ding, Changhong, Zhou, Bo, Guo, Hui, Duan, Yunbao, Wang, Zhenyue
Publicado 2016

Novel Loss-of-Function Variants in CHD2 Cause Childhood-Onset Epileptic Encephalopathy in Chinese Patients

por Wang, Xu, Cui, Di, Ding, Changhong, Chen, Chunhong, Wang, Xiaohui, Fang, Fang, Jin, Hong, Ren, Xiaotun
Publicado 2022

Expanding the mutational spectrum of Rahman syndrome: A rare disorder with severe intellectual disability and particular facial features in two Chinese patients

por Zhao, Jianbo, Lyu, Guizhen, Ding, Changhong, Wang, Xiaohui, Li, Jiuwei, Zhang, Weihua, Yang, Xinying, Zhang, Victor Wei
Publicado 2022

Molecular spectrum of excision repair cross-complementation group 8 gene defects in Chinese patients with Cockayne syndrome type A

por Wang, Xiaozhu, Huang, Yu, Yan, Ming, Li, Jiuwei, Ding, Changhong, Jin, Hong, Fang, Fang, Yang, Yanling, Wu, Baiyan, Chen, Dafang
Publicado 2017

Chinese patients with p.Arg756 mutations of ATP1A3: Clinical manifestations, treatment, and follow‐up

por Zhang, Weihua, Li, Jiuwei, Zhuo, Xiuwei, Zhou, Ji, Feng, Weixing, Gong, Shuai, Ren, Xiaotun, Ding, Changhong, Han, Tongli, Fang, Fang
Publicado 2022

Oculogyric crisis mimicked epilepsy in a Chinese aromatic L-amino acid decarboxylase-deficiency patient: A case report

por Wang, Hongmei, Li, Jiahong, Zhou, Ji, Dai, Lifang, Ding, Changhong, Li, Mo, Feng, Weixing, Fang, Fang, Ren, Xiaotun, Wang, Xiaohui
Publicado 2022

Compound Heterozygous CHAT Gene Mutations of a Large Deletion and a Missense Variant in a Chinese Patient With Severe Congenital Myasthenic Syndrome With Episodic Apnea

por Liu, Zhimei, Zhang, Li, Shen, Danmin, Ding, Changhong, Yang, Xinying, Zhang, Weihua, Li, Jiuwei, Deng, Jie, Gong, Shuai, Liu, Jun, Qian, Suyun, Fang, Fang
Publicado 2019

Clinical Attributes and Electroencephalogram Analysis of Patients With Varying Alpers’ Syndrome Genotypes

por Li, Hua, Wang, Wei, Han, Xiaodi, Zhang, Yujia, Dai, Lifang, Xu, Manting, Deng, Jie, Ding, Changhong, Wang, Xiaohui, Chen, Chunhong, Yang, Xiaofeng, Fang, Fang
Publicado 2021