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An ALS2 gene mutation causes hereditary spastic paraplegia in a Pakistani kindred

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Year: 2002
Type: article
Source: Annals of Neurology
DOI: 10.1002/ana.10422
Authors: François Gros‐Louis, Inge A. Meijer, Collette K. Hand, Marie‐Pierre Dubé, Daune L. MacGregor, Marie‐Hélène Seni, Rebecca S. Devon, Michael R. Hayden, Frederick Andermann, Eva Andermann, Guy A. Rouleau
Institutions: McGill University Health Centre, Research Institute of the McGill University Health Centre, University of Toronto, Hospital for Sick Children, Montreal Neurological Institute and Hospital, McGill University
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

Funder: Canadian Institutes of Health Research
OpenAlex ID: W2104483408
FWCI: 3.428
Cites: 5
Cited by: 111
Related to: 10
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