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 | ||
---|---|---|---|---|---|
3,213 | Dovepress* | 2,949+ | 119 | 3,068 | |
PubMed Central* | 264 | 97 | 361 | ||
Totals | 3,213 | 216 | 3,429 | ||
*Since 4 December 2021 |
Total mentioned | Delicious | Others | |||
---|---|---|---|---|---|
2 | 0 | 0 | 0 | 1 | 1 |
View citations on PubMed Central and Google Scholar