Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A
Year: 2004
Type: article
Study design: Observational Study
Source: Neurogenetics
Institutions: Goethe University Frankfurt, Centre National de la Recherche Scientifique, Génomique Métabolique du Genoscope, Genoscope, Inserm, Pitié-Salpêtrière Hospital, Physiopathologie des Comportements, University of Duisburg-Essen, Assistance Publique – Hôpitaux de Paris, Johannes Gutenberg University Mainz, Guy's Hospital, King's College London
Language: English
Subfield: Cellular and Molecular Neuroscience
Field: Neuroscience
Domain: Life Sciences
Open Access status: closed
Funder: Deutsche Forschungsgemeinschaft
OpenAlex ID: W1992308819