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Mendeley readers
| Title |
Recessive myotonia congenita caused by a homozygous splice site variant in CLCN1 gene: a case report
|
|---|---|
| Published in |
BMC Medical Genomics, October 2020
|
| DOI | 10.1186/s12881-020-01128-5 |
| Pubmed ID | |
| Authors |
Peter Sparber, Margarita Sharova, Alexandra Filatova, Olga Shchagina, Evgeniya Ivanova, Elena Dadali, Mikhail Skoblov |
Mendeley readers
The data shown below were compiled from readership statistics for 16 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
| Country | Count | As % |
|---|---|---|
| Unknown | 16 | 100% |
Demographic breakdown
| Readers by professional status | Count | As % |
|---|---|---|
| Student > Master | 4 | 25% |
| Lecturer | 2 | 13% |
| Unspecified | 1 | 6% |
| Professor | 1 | 6% |
| Other | 1 | 6% |
| Other | 2 | 13% |
| Unknown | 5 | 31% |
| Readers by discipline | Count | As % |
|---|---|---|
| Biochemistry, Genetics and Molecular Biology | 4 | 25% |
| Neuroscience | 2 | 13% |
| Arts and Humanities | 1 | 6% |
| Agricultural and Biological Sciences | 1 | 6% |
| Unspecified | 1 | 6% |
| Other | 2 | 13% |
| Unknown | 5 | 31% |