Autosomal recessive cerebellar ataxia caused by mutations in the PEX2 gene
- DOI
- 10.1186/1750-1172-6-8
- Published
- 2011-03-10
- Container
- Orphanet Journal of Rare Diseases
- Publisher
- Springer Science and Business Media LLC
- Open access
- unknown
Credibility signals
uncertain Score 64/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
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Cite this work
BibTeX
@article{allodium:10.1186/1750-1172-6-8,
title = {Autosomal recessive cerebellar ataxia caused by mutations in the PEX2 gene},
author = {Caroline Sevin and Sacha Ferdinandusse and Hans R Waterham and Ronald J Wanders and Patrick Aubourg},
year = {2011},
journal = {Orphanet Journal of Rare Diseases},
doi = {10.1186/1750-1172-6-8},
url = {https://doi.org/10.1186/1750-1172-6-8}
}RIS
TY - JOUR TI - Autosomal recessive cerebellar ataxia caused by mutations in the PEX2 gene AU - Caroline Sevin AU - Sacha Ferdinandusse AU - Hans R Waterham AU - Ronald J Wanders AU - Patrick Aubourg PY - 2011 JO - Orphanet Journal of Rare Diseases DO - 10.1186/1750-1172-6-8 UR - https://doi.org/10.1186/1750-1172-6-8 ER -
APA
Sevin, C., Ferdinandusse, S., Waterham, H. R., Wanders, R. J., & Aubourg, P. (2011). Autosomal recessive cerebellar ataxia caused by mutations in the PEX2 gene. Orphanet Journal of Rare Diseases. https://doi.org/10.1186/1750-1172-6-8
Source records
- crossref · retrieved 2026-09-26T13:51:45.185Z