Associated Papers
Genetic etiology of 283 Chinese individuals with epilepsy using copy number variation sequencing and whole exome sequencing: a single-center cohort study.
Hu J et al.
Bmc Medical Genomics, 2025
Case Report: De novo variant of the NUS1 gene associated with developmental delay and autism spectrum disorders in a Chinese family.
Ding F et al.
Frontiers in Pediatrics, 2025
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