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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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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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  Data: Prolonged Episodic Dystonia in Tyrosine Hydroxylase Deficiency Due to Homozygous c.698G>A (p.Arg233His) Mutation‐A Diagnostic Challenge.
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  Data: <searchLink fieldCode="JN" term="%22Movement+Disorders+Clinical+Practice%22">Movement Disorders Clinical Practice</searchLink>. Nov2022, Vol. 9 Issue 8, p1136-1139. 4p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=160030026
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        Value: 10.1002/mdc3.13522
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        Text: English
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      – TitleFull: Prolonged Episodic Dystonia in Tyrosine Hydroxylase Deficiency Due to Homozygous c.698G>A (p.Arg233His) Mutation‐A Diagnostic Challenge.
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            NameFull: Uppilli, Bharath Ram
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              Text: Nov2022
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              Y: 2022
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