Xingzhi Chang

3PUBLICATIONS
2CO-AUTHORS
Vision scienceMedical molecular engineering of nucleic acids and proteinsNeurology and neuromuscular diseases
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Publications (3)

|Jan 06, 2022
A new phenotype of syndromic retinitis pigmentosa with myopathy is caused by mutations in retinol dehydrogenase 11.

Yi-Dan Liu, Shu-Shu Huang, Mei Li

|Jul 23, 2021
Centronuclear myopathy due to a de novo nonsense variant and a maternally inherited splice-site variant in TTN: A case report.

Sheng Huang, Yinan Ma, Yu Zhang

|Apr 30, 2021
Clinical and genetic analysis of a case with centronuclear myopathy caused by SPEG gene mutation: a case report and literature review.

Gang Zhang, Min Xu, Tingting Huang

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Frequent Collaborators

2 joint publications

Hui Xiong

1 joint publications

Sheng Huang