Reply to Kremer M et al., The JAK2 V617F mutation occurs frequently in myelodysplastic/myeloproliferative diseases, but is absent in true myelodysplastic syndromes with fibrosis

✍ Scribed by Ohyashiki, K; Ohyashiki, J H

• Book ID: 110056750
• Publisher: Nature Publishing Group
• Year: 2006
• Tongue: English
• Weight: 67 KB
• Volume: 20
• Category: Article
• ISSN: 0887-6924
• DOI: 10.1038/sj.leu.2404232