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Atlastin1 Mutations Are Frequent in Young-Onset Autosomal Dominant Spastic Paraplegia

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Year: 2004
Type: article
Study design: Observational Study
Source: Archives of Neurology
DOI: 10.1001/archneur.61.12.1867
Authors: Alexandra Dürr, Agnès Camuzat, Emilie Colin, Chantal Tallaksen, Didier Hannequin, Paula Coutinho, Bertrand Fontaine, Annick Rossi, Roger Gil, Christophe Rousselle, Merle Ruberg, Giovanni Stevanin, Alexis Brice
Institutions: Inserm, Assistance Publique – Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Physiopathologie des Comportements
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: W2139683636
FWCI: 3.165
Cites: 21
Cited by: 108
Related to: 10
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