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Mendeley readers
Title |
The clinical and mutational spectrum of B3GAT3 linkeropathy: two case reports and literature review
|
---|---|
Published in |
Orphanet Journal of Rare Diseases, June 2019
|
DOI | 10.1186/s13023-019-1110-9 |
Pubmed ID | |
Authors |
Marlies Colman, Tim Van Damme, Elisabeth Steichen-Gersdorf, Franco Laccone, Sheela Nampoothiri, Delfien Syx, Brecht Guillemyn, Sofie Symoens, Fransiska Malfait |
Mendeley readers
The data shown below were compiled from readership statistics for 24 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
Country | Count | As % |
---|---|---|
Unknown | 24 | 100% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Student > Ph. D. Student | 3 | 13% |
Other | 2 | 8% |
Student > Doctoral Student | 2 | 8% |
Professor > Associate Professor | 2 | 8% |
Student > Bachelor | 1 | 4% |
Other | 2 | 8% |
Unknown | 12 | 50% |
Readers by discipline | Count | As % |
---|---|---|
Medicine and Dentistry | 6 | 25% |
Biochemistry, Genetics and Molecular Biology | 2 | 8% |
Nursing and Health Professions | 2 | 8% |
Unspecified | 1 | 4% |
Psychology | 1 | 4% |
Other | 1 | 4% |
Unknown | 11 | 46% |