Phenotypic, Genotypic Characteristics, and Treatment Strategies of Pediatric Tyrosine Hydroxylase Deficiency: A Single‐Center Retrospective Analysis of 51 Cases.

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Title: Phenotypic, Genotypic Characteristics, and Treatment Strategies of Pediatric Tyrosine Hydroxylase Deficiency: A Single‐Center Retrospective Analysis of 51 Cases.
Authors: Ban, Tingting1,2 (AUTHOR), Cheng, Ye3 (AUTHOR), Zhang, Yan1,2 (AUTHOR), Lin, Caimei2 (AUTHOR), Chai, Yiming1 (AUTHOR), Li, Wenhui1 (AUTHOR), Zhang, Linmei1 (AUTHOR), Xing, Qinghe4 (AUTHOR), Wang, Yi1 (AUTHOR), Zhou, Shuizhen1 (AUTHOR) szzhou@shmu.edu.cn
Source: Movement Disorders Clinical Practice. Apr2026, Vol. 13 Issue 4, p907-913. 7p.
Database: Academic Search Ultimate
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  Data: Phenotypic, Genotypic Characteristics, and Treatment Strategies of Pediatric Tyrosine Hydroxylase Deficiency: A Single‐Center Retrospective Analysis of 51 Cases.
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  Data: <searchLink fieldCode="JN" term="%22Movement+Disorders+Clinical+Practice%22">Movement Disorders Clinical Practice</searchLink>. Apr2026, Vol. 13 Issue 4, p907-913. 7p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=192955889
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        Value: 10.1002/mdc3.70371
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      – TitleFull: Phenotypic, Genotypic Characteristics, and Treatment Strategies of Pediatric Tyrosine Hydroxylase Deficiency: A Single‐Center Retrospective Analysis of 51 Cases.
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              Text: Apr2026
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              Y: 2026
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            – TitleFull: Movement Disorders Clinical Practice
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