Xing-Zhi Chang (Xingzhi Chang)

Publication Activity (10 Years)

Years Active: 2021-2022
Publications (10 Years): 3

Top Topics

Mitochondrial Dna

Top Venues

Clinical case reports

Clinical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Yi-Dan Liu, Shu-Shu Huang, Mei Li, Monkol Lek, Dan-Yu Song, Dan-Dan Tan, Xiao-Yu Chen, Hong Zhang, Jie-Yu Liu, Xing-Zhi Chang, Hui Xiong
A new phenotype of syndromic retinitis pigmentosa with myopathy is caused by mutations in retinol dehydrogenase 11. Clinical genetics 101 (4) (2022)
Gang Zhang, Min Xu, Tingting Huang, Wenxin Lin, Jinglin Chen, Wangyang Chen, Xing-Zhi Chang
Clinical and genetic analysis of a case with centronuclear myopathy caused by SPEG gene mutation: a case report and literature review. BMC pediatrics 21 (1) (2021)
Sheng Huang, Yinan Ma, Yu Zhang, Hui Xiong, Xing-Zhi Chang
Centronuclear myopathy due to a de novo nonsense variant and a maternally inherited splice-site variant in TTN: A case report. Clinical case reports 9 (7) (2021)