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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.
Affiliation
  • Panda S; Departments of Neurology All India Institute of Medical Sciences Jodhpur India.
  • Jain S; Departments of Neurology All India Institute of Medical Sciences Jodhpur India.
  • Dholakia D; Genomics and Molecular Medicine CSIR-Institute of Genomics and Integrative Biology Delhi India.
  • Uppilli BR; Genomics and Molecular Medicine CSIR-Institute of Genomics and Integrative Biology Delhi India.
  • Faruq M; Genomics and Molecular Medicine CSIR-Institute of Genomics and Integrative Biology Delhi India.
Mov Disord Clin Pract ; 9(8): 1136-1139, 2022 Nov.
Article in En | MEDLINE | ID: mdl-36339310
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies Language: En Journal: Mov Disord Clin Pract Year: 2022 Document type: Article
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies Language: En Journal: Mov Disord Clin Pract Year: 2022 Document type: Article