Associated Papers
A comparative exploration of monoamine neurotransmitter transport disorders: mechanisms, clinical manifestations, and therapeutic approaches.
Al Sari RR et al.
Journal of Medicine and Life, 2025
A case report of infantile parkinsonism-dystonia-2 caused by homozygous mutation in the SLC18A2 gene.
Zhai H et al.
The International Journal of Neuroscience, 2023
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