CAMK4‐related Case of Hyperkinetic Movement Disorder-Reference-Cited by-同舟云学术

CAMK4‐related Case of Hyperkinetic Movement Disorder

Published:2023-03-03 Issue:4 Volume:10 Page:707-709
ISSN:2330-1619
Container-title:Movement Disorders Clinical Practice
language:en
Short-container-title:Movement Disord Clin Pract

Author:

Alawneh Issa¹,Amburgey Kimberley²³,Gonorazky Hernan¹⁴,Gorodetsky Carolina¹⁵^ORCID

Affiliation:

1. Division of Neurology The Hospital for Sick Children Toronto Ontario Canada

2. Division of Neurology, Department of Pediatrics, The Hospital for Sick Children University of Toronto Toronto Ontario Canada

3. Department of Molecular Genetics University of Toronto Toronto Ontario Canada

4. Division of Neurology, Department of Pediatrics, The Hospital for Sick Children. Program for Genetics and Genome Biology, The Hospital for Sick Children University of Toronto Toronto Ontario Canada

5. Department of pediatrics University of Toronto Toronto Ontario Canada

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mdc3.13702

Reference8 articles.

1. De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability

2. Ca2+/Calmodulin-dependent Protein Kinases

3. Convergent CaMK and RacGEF signals control dendritic structure and function

4. Calmodulin kinases: essential regulators in health and disease

5. A unique de novo gain-of-function variant in CAMK4 associated with intellectual disability and hyperkinetic movement disorder

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