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Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

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Year: 1999
Type: article
Study design: Observational Study
Source: Nature Genetics
DOI: 10.1038/15472
Authors: Jamilé Hazan, Nùria Fonknechten, Delphine Mavel, Caroline Paternotte, Delphine Samson, François Artiguenave, Claire-Sophie Davoine, Corinne Cruaud, Alexandra Dürr, Patrick Wincker, Philippe Brottier, Laurence Cattolico, Valérie Barbe, Jean-Marc Burgunder, Jean-François Prud'homme, Alexis Brice, Bertrand Fontaine, Roland Heilig, Jean Weissenbach
Institutions: Genoscope, Inserm, Pitié-Salpêtrière Hospital, Physiopathologie des Comportements, University of Bern, University Hospital of Bern, Genethon (France)
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: W1498629854
FWCI: 9.807
Cites: 53
Cited by: 633
Related to: 10
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