Associated Papers
The genetic spectrum features of 2261 Chinese children with epilepsy and intellectual disability.
Pang N et al.
Bmc Medicine, 2025
40598568 (PubMed )
Supplement: 12916_2025_4220_MOESM1_ESM.xlsx › Table_S3
SYN1 variant causes X-linked neurodevelopmental disorders: a case report of variable clinical phenotypes in siblings.
Ren B et al.
Frontiers in Neurology, 2024
The different clinical facets of SYN1-related neurodevelopmental disorders.
Parenti I et al.
Frontiers in Cell and Developmental Biology, 2022
Familial SYN1 variants related neurodevelopmental disorders in Asian pediatric patients.
Xiong J et al.
Bmc Medical Genomics, 2021
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