Work

Inactivation of the peroxisomal ABCD2 transporter in the mouse leads to late-onset ataxia involving mitochondria, Golgi and endoplasmic reticulum damage

Year: 2005

Type: article

Source: Human Molecular Genetics

DOI: 10.1093/hmg/ddi384

Authors: Isidre Ferrer, Josef P. Kapfhammer, Colette Hindelang, Stephan Kemp, Nathalie Troffer-Charlier, Vania Broccoli, Noëlle Callyzot, Petra Mooyer, Jacqueline Selhorst, Peter Vreken, Ronald J.A. Wanders, Jean Louis Mandel, Aurora Pujol

Institutions: Bellvitge University Hospital, Universitat de Barcelona, University of Basel, Centre National de la Recherche Scientifique, Inserm, Collège de France, Institut de génétique et de biologie moléculaire et cellulaire, Amsterdam UMC Location University of Amsterdam, Emma Kinderziekenhuis, University of Amsterdam, Sig Holding (Switzerland), Neurophet (South Korea), Université de Strasbourg, Institució Catalana de Recerca i Estudis Avançats

Language: English

Topic: Metabolism and Genetic Disorders

Subfield: Clinical Biochemistry

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: European Commission, Centre National de la Recherche Scientifique, Association Européenne contre les Leucodystrophies

OpenAlex ID: W2099862428

FWCI: 4.375

Cites: 55

Cited by: 105

Related to: 10