Publication | Closed Access
<scp>JAK</scp>2 <scp>V</scp>617<scp>F</scp> mutation and 46/1 haplotype in <scp>C</scp>hinese <scp>B</scp>udd‐<scp>C</scp>hiari syndrome patients
35
Citations
31
References
2013
Year
Our study showed that the presence of 46/1 haplotype increased the risk of JAK2V617F-positive BCS in China. In addition, low prevalence of JAK2V617F mutation in BCS patients suggested that myeloproliferative neoplasms (MPNs) should not be an etiological factor of BCS in China.
| Year | Citations | |
|---|---|---|
Page 1
Page 1