Work

Mutation analysis of the paraplegin gene ( SPG7 ) in patients with hereditary spastic paraplegia

Year: 2006

Type: article

Study design: Observational Study

Source: Neurology

DOI: 10.1212/01.wnl.0000201185.91110.15

Authors: N. Elleuch, C. Depienne, A. Benomar, A. M. Ouvrard Hernandez, X. Ferrer, B. Fontaine, D. Grid, C.M.E. Tallaksen, R. Zemmouri, G. Stevanin, A. Durr, A. Brice

Institutions: Inserm, Centre Hospitalier Universitaire de Grenoble, Centre Hospitalier Universitaire de Bordeaux, Pitié-Salpêtrière Hospital, Université Pierre-et-Marie-Curie

Language: English

Topic: Hereditary Neurological Disorders

Subfield: Cellular and Molecular Neuroscience

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2108524651

FWCI: 3.417

Cites: 14

Cited by: 106

Related to: 10