Marked variation in clinical presentation and age of onset in a family with a heterozygous parkin mutation
Year: 2003
Type: article
Study design: Case Report
Source: Movement Disorders
DOI: 10.1002/mds.10432
Language: English
Subfield: Clinical Neurology
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W2054818048
