ADCY5 Related Dyskinesia—A Rare Mutation
Author:
Affiliation:
1. Department of Neurology, Institute of Medical Science Banaras Hindu University Varanasi India
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/mdc3.13419
Reference8 articles.
1. Autosomal Dominant Familial Dyskinesia and Facial Myokymia
2. Differential Expression of Type I, II, and V Adenylyl Cyclase Gene in the Postnatal Developing Rat Brain
3. A de novo ADCY5 mutation causes early‐onset autosomal dominant chorea and dystonia
4. Phenotypic insights into ADCY5 ‐associated disease
5. Autosomal recessive inheritance of ADCY5-related generalized dystonia and myoclonus
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1. Investigating neuropathological changes and underlying neurobiological mechanisms in the early stages of primary blast-induced traumatic brain injury: Insights from a rat model;Experimental Neurology;2024-05
2. ADCY5-related dyskinesias: An amalgamation of various hyperkinetic movement disorders;Annals of Movement Disorders;2024-03-21
3. Scoping Review onADCY5‐Related Movement Disorders;Movement Disorders Clinical Practice;2023-06-06
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