APA (7th ed.) Citation

Panda, S., Jain, S., Dholakia, D., Uppilli, B. R., & Faruq, M. (2022). Prolonged Episodic Dystonia in Tyrosine Hydroxylase Deficiency Due to Homozygous c.698G>A (p.Arg233His) Mutation‐A Diagnostic Challenge. Movement Disorders Clinical Practice, 9(8), 1136. https://doi.org/10.1002/mdc3.13522

Chicago Style (17th ed.) Citation

Panda, Samhita, Saksham Jain, Dhwani Dholakia, Bharath Ram Uppilli, and Mohammed Faruq. "Prolonged Episodic Dystonia in Tyrosine Hydroxylase Deficiency Due to Homozygous C.698G>A (p.Arg233His) Mutation‐A Diagnostic Challenge." Movement Disorders Clinical Practice 9, no. 8 (2022): 1136. https://doi.org/10.1002/mdc3.13522.

MLA (9th ed.) Citation

Panda, Samhita, et al. "Prolonged Episodic Dystonia in Tyrosine Hydroxylase Deficiency Due to Homozygous C.698G>A (p.Arg233His) Mutation‐A Diagnostic Challenge." Movement Disorders Clinical Practice, vol. 9, no. 8, 2022, p. 1136, https://doi.org/10.1002/mdc3.13522.