Li Yang
5PUBLICATIONS
2CO-AUTHORS
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Publications (5)
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|Jan 20, 2026
Multiple Mitochondrial Dysfunction Syndrome Caused by IBA57 Gene Mutation: A Case Report and Literature Review.Jia Xu, Xin Zhang, Ying Hua
|Aug 14, 2024
Clinical and genetic analysis of 23 Chinese children with epilepsy associated with KCNQ2 gene mutations.Xixi Yu, Fengyuan Che, Xin Zhang
|Feb 07, 2023
A novel heterozygous ATP1A2 pathogenic variant in a Chinese child with MELAS-like alternating hemiplegia.Xin Zhang, Shiyan Qiu, Li Yang
|Aug 11, 2020
A novel composition of two heterozygous GFM1 mutations in a Chinese child with epilepsy and mental retardation.Cuiping You, Na Xu, Shiyan Qiu
|Apr 03, 2020
Novel and de novo point and large microdeletion mutation in PRRT2-related epilepsy.Li Yang, Cuiping You, Shiyan Qiu
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