𝔖 Bobbio Scriptorium
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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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