Mutation Analysis of SPG4 and SPG3A Genes and Its Implication in Molecular Diagnosis of Korean Patients With Hereditary Spastic Paraplegia
Year: 2005
Type: article
Study design: Observational Study
Source: Archives of Neurology
Institutions: Samsung Medical Center, Sungkyunkwan University
Language: English
Subfield: Cellular and Molecular Neuroscience
Field: Neuroscience
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2134316644
