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Revisado por pares
The S505A thrombopoietin receptor mutation in childhood hereditary thrombocytosis and essential thrombocythemia is S505N: single letter amino acid code matters
2019; Springer Nature; Volume: 33; Issue: 2 Linguagem: Inglês
10.1038/s41375-018-0356-x
ISSN1476-5551
AutoresJean‐Philippe Defour, Gabriel Levy, Emilie Leroy, Steven O. Smith, Stefan N. Constantinescu,
Tópico(s)Kruppel-like factors research
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