| Title |
Loss-of-function mutation in inositol monophosphatase 1 (IMPA1) results in abnormal synchrony in resting-state EEG
|
|---|---|
| Published in |
Orphanet Journal of Rare Diseases, January 2019
|
| DOI | 10.1186/s13023-018-0977-1 |
| Pubmed ID | |
| Authors |
Christopher P. Walker, Andre L. S. Pessoa, Thalita Figueiredo, Megan Rafferty, Uirá S. Melo, Paulo R. Nóbrega, Nicholas Murphy, Fernando Kok, Mayana Zatz, Silvana Santos, Raymond Y. Cho |
Mendeley readers
The data shown below were compiled from readership statistics for 29 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
| Country | Count | As % |
|---|---|---|
| Unknown | 29 | 100% |
Demographic breakdown
| Readers by professional status | Count | As % |
|---|---|---|
| Student > Master | 4 | 14% |
| Researcher | 4 | 14% |
| Student > Bachelor | 3 | 10% |
| Student > Ph. D. Student | 2 | 7% |
| Other | 1 | 3% |
| Other | 2 | 7% |
| Unknown | 13 | 45% |
| Readers by discipline | Count | As % |
|---|---|---|
| Neuroscience | 4 | 14% |
| Medicine and Dentistry | 3 | 10% |
| Psychology | 3 | 10% |
| Biochemistry, Genetics and Molecular Biology | 2 | 7% |
| Nursing and Health Professions | 2 | 7% |
| Other | 2 | 7% |
| Unknown | 13 | 45% |