Clinical approach to monogenic Parkinson's disease
Clinical approach to monogenic Parkinson's disease
About this item
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Publisher
India: Wolters Kluwer - Medknow
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Language
English
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Publisher
India: Wolters Kluwer - Medknow
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Scope and Contents
Contents
Abstract
Monogenic Parkinson's disease refers to the Parkinson's disease phenotype caused by mutations in genes that generally follow a mendelian pattern of inheritance. Though this is a rare entity in comparison to idiopathic Parkinson's disease, they provide an opportunity to understand the pathophysiological basis of this neurodegenerative di...
Alternative Titles
Full title
Clinical approach to monogenic Parkinson's disease
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TN_cdi_doaj_primary_oai_doaj_org_article_64ebb87b77a54a029c4cbdef802bc872
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_64ebb87b77a54a029c4cbdef802bc872
Other Identifiers
ISSN
2590-3446
E-ISSN
2590-3454
DOI
10.4103/aomd.aomd_100_24