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Mendeley readers
| Title |
Whole-exome sequencing identifies a novel missense variant within LOXHD1 causing rare hearing loss in a Chinese family
|
|---|---|
| Published in |
BMC Medical Genomics, February 2019
|
| DOI | 10.1186/s12881-019-0758-2 |
| Pubmed ID | |
| Authors |
Na Shen, Ting Wang, Delei Li, Aiguo Liu, Yanjun Lu |
Mendeley readers
The data shown below were compiled from readership statistics for 26 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
| Country | Count | As % |
|---|---|---|
| Unknown | 26 | 100% |
Demographic breakdown
| Readers by professional status | Count | As % |
|---|---|---|
| Unspecified | 4 | 15% |
| Student > Ph. D. Student | 3 | 12% |
| Researcher | 3 | 12% |
| Student > Doctoral Student | 2 | 8% |
| Student > Master | 1 | 4% |
| Other | 3 | 12% |
| Unknown | 10 | 38% |
| Readers by discipline | Count | As % |
|---|---|---|
| Unspecified | 4 | 15% |
| Biochemistry, Genetics and Molecular Biology | 3 | 12% |
| Neuroscience | 2 | 8% |
| Agricultural and Biological Sciences | 2 | 8% |
| Nursing and Health Professions | 1 | 4% |
| Other | 2 | 8% |
| Unknown | 12 | 46% |