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Li Yang

5PUBLICATIONS

2CO-AUTHORS

Medical mycologyNeonatologyGene and molecular therapyEpigenetics (incl. genome methylation and epigenomics)Infant and child health

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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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Frequent Collaborators

1 joint publications

Baomin Li

1 joint publications

Jia Xu

Frequent Collaborators

1 joint publications

Baomin Li

1 joint publications

Jia Xu

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