Benign Hereditary Chorea as a Manifestation of <scp>HPCA</scp> Mutation-Reference-Cited by-同舟云学术

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Benign Hereditary Chorea as a Manifestation of HPCA Mutation

Published:2022-10-10 Issue:1 Volume:10 Page:130-134
ISSN:2330-1619
Container-title:Movement Disorders Clinical Practice
language:en
Short-container-title:Movement Disord Clin Pract

Author:

Brunetti Sara¹^ORCID,Micheletti Serena¹^ORCID,Palmieri Ilaria²^ORCID,Valente Enza Maria²³^ORCID,Fazzi Elisa¹⁴^ORCID

Affiliation:

1. Unit of Child Neurology and Psychiatry ASST Spedali Civili of Brescia Brescia Italy

2. Neurogenetics Research Center IRCCS Mondino Foundation Pavia Italy

3. Department of Molecular Medicine University of Pavia Pavia Italy

4. Department of Clinical and Experimental Sciences University of Brescia Brescia Italy

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mdc3.13572

Reference24 articles.

1. Mutations in HPCA Cause Autosomal-Recessive Primary Isolated Dystonia

2. HPCA confirmed as a genetic cause of DYT2-like dystonia phenotype

4. DYT2 screening in early-onset isolated dystonia

5. Specific Cognitive Changes due to Hippocalcin Alterations? A Novel Familial Homozygous Hippocalcin Variant Associated with Inherited Dystonia and Altered Cognition

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Recent advances in non-Huntington's disease choreas;Parkinsonism & Related Disorders;2024-05

2. Pallidal Deep Brain Stimulation Improves HPCA‐Linked (DYT 2) Dystonia;Movement Disorders Clinical Practice;2023-12-20

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