Work

NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe

Year: 2007

Type: article

Source: Neurogenetics

DOI: 10.1007/s10048-006-0074-9

Authors: Stephan Klebe, Arnaud Lacour, Alexandra Durr, Tanya Stojkovic, Christel Depienne, Sylvie Forlani, Sandrine Poea-Guyon, Isabelle Vuillaume, Bernard Sablonniere, Patrick Vermersch, Alexis Brice, Giovanni Stevanin

Institutions: Inserm, Pitié-Salpêtrière Hospital, Université Pierre-et-Marie-Curie, Hôpital Roger Salengro, Assistance Publique – Hôpitaux de Paris

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

Funders: Stiftung VERUM, Deutscher Akademischer Austauschdienst

OpenAlex ID: W2082250497

FWCI: 0.794

Cites: 6

Cited by: 26

Related to: 10