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Prolonged Episodic Dystonia in Tyrosine Hydroxylase Deficiency Due to Homozygous c.698G>A (p.Arg233His) Mutation‐A Diagnostic Challenge.

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Bibliographic Details
Title:	Prolonged Episodic Dystonia in Tyrosine Hydroxylase Deficiency Due to Homozygous c.698G>A (p.Arg233His) Mutation‐A Diagnostic Challenge.
Authors:	Panda, Samhita¹ (AUTHOR) samhitapanda@yahoo.com, Jain, Saksham¹ (AUTHOR), Dholakia, Dhwani² (AUTHOR), Uppilli, Bharath Ram² (AUTHOR), Faruq, Mohammed² (AUTHOR)
Source:	Movement Disorders Clinical Practice. Nov2022, Vol. 9 Issue 8, p1136-1139. 4p.
Database:	Academic Search Ultimate
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Description
ISSN:	23301619
DOI:	10.1002/mdc3.13522