Ban, T., Cheng, Y., Zhang, Y., Lin, C., Chai, Y., Li, W., . . . Zhou, S. (2026). Phenotypic, Genotypic Characteristics, and Treatment Strategies of Pediatric Tyrosine Hydroxylase Deficiency: A Single‐Center Retrospective Analysis of 51 Cases. Movement Disorders Clinical Practice, 13(4), 907. https://doi.org/10.1002/mdc3.70371
Chicago Style (17th ed.) CitationBan, Tingting, et al. "Phenotypic, Genotypic Characteristics, and Treatment Strategies of Pediatric Tyrosine Hydroxylase Deficiency: A Single‐Center Retrospective Analysis of 51 Cases." Movement Disorders Clinical Practice 13, no. 4 (2026): 907. https://doi.org/10.1002/mdc3.70371.
MLA (9th ed.) CitationBan, Tingting, et al. "Phenotypic, Genotypic Characteristics, and Treatment Strategies of Pediatric Tyrosine Hydroxylase Deficiency: A Single‐Center Retrospective Analysis of 51 Cases." Movement Disorders Clinical Practice, vol. 13, no. 4, 2026, p. 907, https://doi.org/10.1002/mdc3.70371.