Work

Novel SPG 10 mutation associated with dysautonomia, spinal cord atrophy, and skin biopsy abnormality

Year: 2012

Type: article

Study design: Case Report

Source: European Journal of Neurology

DOI: 10.1111/j.1468-1331.2012.03803.x

Authors: N. Collongues, C. Depienne, N. Boehm, A. Echaniz‐Laguna, B. Samama, A. Dürr, G. Stevanin, E. Leguern, A. Brice, P. Labauge, J. de Seze

Institutions: Université de Strasbourg, Centre National de la Recherche Scientifique, Inserm, Assistance Publique – Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Institut du Cerveau, Université Pierre-et-Marie-Curie, Université de Montpellier

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: W2002694210

FWCI: 0.659

Cites: 9

Cited by: 10

Related to: 10