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Mendeley readers
| Title |
Autosomal recessive cerebellar ataxia caused by mutations in the PEX2 gene
|
|---|---|
| Published in |
Orphanet Journal of Rare Diseases, March 2011
|
| DOI | 10.1186/1750-1172-6-8 |
| Pubmed ID | |
| Authors |
Caroline Sevin, Sacha Ferdinandusse, Hans R Waterham, Ronald J Wanders, Patrick Aubourg |
Mendeley readers
The data shown below were compiled from readership statistics for 52 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
| Country | Count | As % |
|---|---|---|
| Netherlands | 1 | 2% |
| Germany | 1 | 2% |
| Unknown | 50 | 96% |
Demographic breakdown
| Readers by professional status | Count | As % |
|---|---|---|
| Researcher | 11 | 21% |
| Student > Ph. D. Student | 8 | 15% |
| Professor | 5 | 10% |
| Student > Bachelor | 5 | 10% |
| Other | 3 | 6% |
| Other | 10 | 19% |
| Unknown | 10 | 19% |
| Readers by discipline | Count | As % |
|---|---|---|
| Biochemistry, Genetics and Molecular Biology | 13 | 25% |
| Medicine and Dentistry | 11 | 21% |
| Agricultural and Biological Sciences | 10 | 19% |
| Neuroscience | 3 | 6% |
| Unspecified | 1 | 2% |
| Other | 2 | 4% |
| Unknown | 12 | 23% |