Associated Papers
SLC18A2 associated infantile-onset- parkinsonism-dystonia 2: A novel genotype.
Janardhanan A et al.
Parkinsonism & Related Disorders, 2025
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
Novel SLC18A2 Variant in Infantile Dystonia-Parkinsonism Type 2.
Kaasalainen S et al.
Case Reports in Neurological Medicine, 2024
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