Goldman, J. S., Uhlmann, W. R., Naini, A. B., Klitzman, R. L., & Marder, K. S. (2023). Genetic Testing of HTT Modifiers for Huntington’s Disease: Considerations for Clinical Guidelines. Movement Disorders, 38(12), 2151–2154. Portico. https://doi.org/10.1002/mds.29650
Subjects:
Molecular Mechanisms of Neurodegenerative Diseases
(OpenAlex Topic)
Deep Brain Stimulation for Neurological Disorders
(OpenAlex Topic)
Diagnosis and Management of Hypertrophic Cardiomyopathy
(OpenAlex Topic)
Huntington Disease
(MeSH)
Publication Type:
Article
Unique ID:
10.1002/mds.29650
PMID:
DOI:
Journal:
Publication Date:
Data Source:
PubMed
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