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Mendeley readers
| Title |
A L2HGDH initiator methionine codon mutation in a Yorkshire terrier with L-2-hydroxyglutaric aciduria
|
|---|---|
| Published in |
BMC Veterinary Research, July 2012
|
| DOI | 10.1186/1746-6148-8-124 |
| Pubmed ID | |
| Authors |
Fabiana HG Farias, Rong Zeng, Gary S Johnson, G D Shelton, Dominique Paquette, Dennis P O’Brien |
| Abstract |
L-2-hydroxyglutaric aciduria is a metabolic repair deficiency characterized by elevated levels of L-2-hydroxyglutaric acid in urine, blood and cerebrospinal fluid. Neurological signs associated with the disease in humans and dogs include seizures, ataxia and dementia. |
Mendeley readers
The data shown below were compiled from readership statistics for 41 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
| Country | Count | As % |
|---|---|---|
| Unknown | 41 | 100% |
Demographic breakdown
| Readers by professional status | Count | As % |
|---|---|---|
| Student > Bachelor | 6 | 15% |
| Other | 4 | 10% |
| Student > Ph. D. Student | 4 | 10% |
| Researcher | 4 | 10% |
| Student > Postgraduate | 3 | 7% |
| Other | 12 | 29% |
| Unknown | 8 | 20% |
| Readers by discipline | Count | As % |
|---|---|---|
| Veterinary Science and Veterinary Medicine | 13 | 32% |
| Agricultural and Biological Sciences | 4 | 10% |
| Medicine and Dentistry | 4 | 10% |
| Psychology | 4 | 10% |
| Biochemistry, Genetics and Molecular Biology | 3 | 7% |
| Other | 4 | 10% |
| Unknown | 9 | 22% |