Genetic heterogeneity of early onset Parkinson disease: The dilemma of clinico-genetic correlation

With advances in genetic testing increasing proportion of early onset Parkinson disease (EOPD) are being identified to have an underlying genetic aetiology. This is can be in the form of either highly penetrant genes associated with phenotypes with monogenic or mendelian inheritance patterns or thos...

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Veröffentlicht in:	Parkinsonism & related disorders 2024-12, Vol.129, p.107146, Article 107146
Hauptverfasser:	Rajan, Roopa, Holla, Vikram V., Kamble, Nitish, Yadav, Ravi, Pal, Pramod Kumar
Format:	Artikel
Sprache:	eng
Schlagworte:	Age of Onset alpha-Synuclein - genetics Genetic Association Studies Genetic Heterogeneity Genetic Predisposition to Disease Humans Parkinson Disease - genetics Parkinson Disease - physiopathology Phenotype Ubiquitin-Protein Ligases
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