Associated Papers
Phenotypic, Genotypic Characteristics, and Treatment Strategies of Pediatric Tyrosine Hydroxylase Deficiency: A Single-Center Retrospective Analysis of 51 Cases.
Ban T et al.
Movement Disorders Clinical Practice, 2025
Identification of TH Variants in Chinese Dopa-Responsive Dystonia Patients and Long-Term Outcomes.
Li XY et al.
Frontiers in Neurology, 2021
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