Europe PMCopen access
Exploring cerebral small vessel disease signatures in familial Parkinson's disease
Parkinson’s Disease (Pd), Vascular Parkinsonism (Vp), Parkinson Mendelian Genes, Whole Exome Sequencing (Wes)., Cerebral Small Vessel Disease (Csvd), White Matter Hyperintensities (Wmh)
This document is indexed with metadata only — full text is not available in the archive for this record.
Open the official source ↗
Record · ID 784523
Retrieved via
Conceptio — every document is proof-bundled with source, license, and retrieval metadata.