Familial SYN1 variants related neurodevelopmental disorders in Asian pediatric patients

Abstract Background SYN1 encodes synapsin I, which is a neuronal phosphoprotein involving in regulating axonogenesis and synaptogenesis. Variants in the gene have been associated with X-linked neurodevelopmental disorders in recent years. Methods In the study, we reported two male patients with fami...

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Main Authors: Juan Xiong (Author), Haolin Duan (Author), Shimeng Chen (Author), Miriam Kessi (Author), Fang He (Author), Xiaolu Deng (Author), Ciliu Zhang (Author), Li Yang (Author), Jing Peng (Author), Fei Yin (Author)
Format: Book
Published: BMC, 2021-07-01T00:00:00Z.
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