Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia
Year: 2000
Type: article
Study design: Observational Study
Source: Human Molecular Genetics
DOI: 10.1093/hmg/9.4.637
Author: N. Fonknechten
Language: English
Subfield: Cellular and Molecular Neuroscience
Field: Neuroscience
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2110378485