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Clinical approach to monogenic Parkinson's disease

Clinical approach to monogenic Parkinson's disease

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_64ebb87b77a54a029c4cbdef802bc872

Clinical approach to monogenic Parkinson's disease

About this item

Full title

Clinical approach to monogenic Parkinson's disease

Author / Creator

Publisher

India: Wolters Kluwer - Medknow

Journal title

Annals of movement disorders, 2025, Vol.8 (1), p.1-13

Language

English

Formats

Publication information

Publisher

India: Wolters Kluwer - Medknow

More information

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

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

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

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