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CALR exon 9 mutations are somatically acquired events in familial cases of essential thrombocythemia or primary myelofibrosis

✍ Scribed by Rumi, E.; Harutyunyan, A. S.; Pietra, D.; Milosevic, J. D.; Casetti, I. C.; Bellini, M.; Them, N. C. C.; Cavalloni, C.; Ferretti, V. V.; Milanesi, C.; Berg, T.; Sant'Antonio, E.; Boveri, E.; Pascutto, C.; Astori, C.; Kralovics, R.; Cazzola, M.


Book ID
121793593
Publisher
American Society of Hematology
Year
2014
Tongue
English
Weight
612 KB
Volume
123
Category
Article
ISSN
0006-4971

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