Work

Ataxia with isolated vitamin E deficiency is caused by mutations in the α–tocopherol transfer protein

Year: 1995

Type: article

Study design: Observational Study

Source: Nature Genetics

DOI: 10.1038/ng0295-141

Authors: Karim Ouahchi, Makoto Arita, Herbert Kayden, Fayçal Hentati, Mongi Ben Hamida, Ronald Sokol, Hiroyuki Arai, Keizo Inoue, Jean-Louis Mandel, Michel Koenig

Institutions: Centre National de la Recherche Scientifique, Inserm, Institut de génétique et de biologie moléculaire et cellulaire, NYU Langone Health, University of Colorado Anschutz, University of Colorado Denver, Hôpitaux Universitaires de Strasbourg

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: green

Funders: National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases, National Center for Research Resources

Awards: HEPATOBILIARY CENTER, General Clinical Research Center, G980352038

OpenAlex ID: W2050244960

FWCI: 9.07

Cites: 31

Cited by: 577

Related to: 10