Inactivation of the peroxisomal ABCD2 transporter in the mouse leads to late-onset ataxia involving mitochondria, Golgi and endoplasmic reticulum damage.
- DOI
- 10.1093/hmg/ddi384
- Published
- 2005 Dec 1
- Container
- Human molecular genetics
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1093/hmg/ddi384,
title = {Inactivation of the peroxisomal ABCD2 transporter in the mouse leads to late-onset ataxia involving mitochondria, Golgi and endoplasmic reticulum damage.},
author = {Ferrer I and Kapfhammer JP and Hindelang C and Kemp S and Troffer-Charlier N and Broccoli V and Callyzot N and Mooyer P and Selhorst J and Vreken P and Wanders RJ and Mandel JL and Pujol A},
year = {2005},
journal = {Human molecular genetics},
doi = {10.1093/hmg/ddi384},
url = {https://doi.org/10.1093/hmg/ddi384}
}RIS
TY - JOUR TI - Inactivation of the peroxisomal ABCD2 transporter in the mouse leads to late-onset ataxia involving mitochondria, Golgi and endoplasmic reticulum damage. AU - Ferrer I AU - Kapfhammer JP AU - Hindelang C AU - Kemp S AU - Troffer-Charlier N AU - Broccoli V AU - Callyzot N AU - Mooyer P AU - Selhorst J AU - Vreken P AU - Wanders RJ AU - Mandel JL AU - Pujol A PY - 2005 JO - Human molecular genetics DO - 10.1093/hmg/ddi384 UR - https://doi.org/10.1093/hmg/ddi384 ER -
APA
I, F., JP, K., C, H., S, K., N, T., V, B., N, C., P, M., J, S., P, V., RJ, W., JL, M., & A, P. (2005). Inactivation of the peroxisomal ABCD2 transporter in the mouse leads to late-onset ataxia involving mitochondria, Golgi and endoplasmic reticulum damage.. Human molecular genetics. https://doi.org/10.1093/hmg/ddi384
Source records
- pubmed · retrieved 2026-09-25T05:23:06.735Z