Work

A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21

Year: 2007

Type: article

Study design: Observational Study

Source: Neurology

DOI: 10.1212/01.wnl.0000262043.53386.22

Authors: G. Stevanin, C. Paternotte, P. Coutinho, S. Klebe, N. Elleuch, J. L. Loureiro, E. Denis, V. T. Cruz, A. Dürr, J.-F Prud’homme, J. Weissenbach, A. Brice, J. Hazan

Institutions: Inserm, Assistance Publique – Hôpitaux de Paris, Genoscope, 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: W2037292742

FWCI: 1.456

Cites: 9

Cited by: 35

Related to: 10