Old Web
English
Sign In
Acemap
>
authorDetail
>
Yuan Huijun
Yuan Huijun
Southwest General Health Center
Medicine
SOX10
Genetics
Mutation
Hearing loss
2
Papers
0
Citations
0
KQI
Citation Trend
Filter By
Interval:
1900~2024
1900
2024
Author
Papers (2)
Sort By
Default
Most Recent
Most Early
Most Citation
No data
Journal
Conference
Others
Two novel BTD mutations causing profound biotinidase deficiency in a Chinese patient
2021
Molecular Genetics & Genomic Medicine
Jia Geng
Yi. Sun
Yi Zhao
Wenyu Xiong
Mingjun Zhong
Yajuan Zhang
Qiuling Zhao
Zhongwei Bao
Jing Cheng
Yu Lu
Yuan Huijun
Show All
Source
Cite
Save
Citations (0)
A follow-up study of a Chinese family with Waardenburg syndrome type II caused by a truncating mutation of MITF gene.
2020
Molecular Genetics & Genomic Medicine
Shu-Zhi Yang
Cuicui Wang
Chengyong Zhou
Dongyang Kang
Xin Zhang
Yuan Huijun
Show All
Source
Cite
Save
Citations (0)
1