A case of complicated spastic paraplegia 2 due to a point mutation in the proteolipid protein 1 gene
Year: 2004
Type: article
Study design: Case Report
Language: English
Subfield: Cellular and Molecular Neuroscience
Field: Neuroscience
Domain: Life Sciences
Open Access status: closed
Funder: National Institutes of Health
OpenAlex ID: W1993059727
