✦ LIBER ✦
P-040 SRSF2 mutation is associated with CMML but its clinical significance remains obscure
✍ Scribed by Zhang, S.; Yang, X.; Qian, S.; Li, J.
- Book ID
- 122882783
- Publisher
- Elsevier Science
- Year
- 2013
- Tongue
- English
- Weight
- 70 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0145-2126
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