Prolonged Episodic Dystonia in Tyrosine Hydroxylase Deficiency Due to Homozygous c.698G>A (p.Arg233His) Mutation‐A Diagnostic Challenge. - Panda, Samhita; Jain, Saksham; Dholakia, Dhwani; Uppilli, Bharath Ram; Faruq, Mohammed (Movement Disorders Clinical Practice, 2022)