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<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

Abstract

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.

References

YearCitations

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