Menu
Back to Journals » Pharmacogenomics and Personalized Medicine » Volume 14
Case report
Identification of a Novel VPS13B Mutation in a Chinese Patient with Cohen Syndrome by Whole-Exome Sequencing
| Total article views | HTML views | PDF downloads | Totals | ||
|---|---|---|---|---|---|
| 3,150 | Dovepress* | 2,892+ | 118 | 3,010 | |
| PubMed Central* | 258 | 96 | 354 | ||
| Totals | 3,150 | 214 | 3,364 | ||
| *Since 4 December 2021 | |||||
| Total mentioned | Delicious | Others | |||
|---|---|---|---|---|---|
| 2 | 0 | 0 | 0 | 1 | 1 |
View citations on PubMed Central and Google Scholar