Work

Novel missense mutation in the early growth response 2 gene associated with Dejerine–Sottas syndrome phenotype

Year: 1999

Type: article

Study design: Observational Study

Source: Neurology

DOI: 10.1212/wnl.52.9.1827

Authors: V. Timmerman, P. De Jonghe, C. Ceuterick, E. De Vriendt, A. Löfgren, E. Nelis, L.E. Warner, J.R. Lupski, J.-J. Martin, C. Van Broeckhoven

Institutions: University of Antwerp, Baylor College of Medicine, Antwerp University Hospital

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: W2040394644

FWCI: 6.096

Cites: 20

Cited by: 158

Related to: 10