Menu
Back to Journals » The Application of Clinical Genetics » Volume 10
Case report
Novel mutation of FKBP10 in a pediatric patient with osteogenesis imperfecta type XI identified by clinical exome sequencing
| Total article views | HTML views | PDF downloads | Totals | ||
|---|---|---|---|---|---|
| 8,171 | Dovepress* | 7,583+ | 1,338 | 8,921 | |
| PubMed Central* | 588 | 221 | 809 | ||
| Totals | 8,171 | 1,559 | 9,730 | ||
| *Since 7 November 2017 | |||||
| Total mentioned | Delicious | Others | |||
|---|---|---|---|---|---|
| 2 | 0 | 0 | 0 | 1 | 1 |
View citations on PubMed Central and Google Scholar