Work

A new locus (SPG46) maps to 9p21.2-q21.12 in a Tunisian family with a complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum

Year: 2010

Type: article

Study design: Observational Study

Source: Neurogenetics

DOI: 10.1007/s10048-010-0249-2

Authors: Amir Boukhris, Imed Feki, Nizar Elleuch, Mohamed Imed Miladi, Anne Boland-Augé, Jérémy Truchetto, Emeline Mundwiller, Nadia Jezequel, Diana Zelenika, Chokri Mhiri, Alexis Brice, Giovanni Stevanin

Institutions: Hopital Universitaire Habib Bourguiba, Faculty of Medicine of Sfax, Centre National de la Recherche Scientifique, Inserm, Pitié-Salpêtrière Hospital, Institut du Cerveau, Université Pierre-et-Marie-Curie, Assistance Publique – Hôpitaux de Paris, École Pratique des Hautes Études

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: Agence Nationale de la Recherche, CHIST-ERA

OpenAlex ID: W1980714413

FWCI: 2.194

Cites: 32

Cited by: 53

Related to: 10