The S505A thrombopoietin receptor mutation in childhood hereditary thrombocytosis and essential thrombocythemia is S505N: single letter amino acid code matters.

Leukemia

Université catholique de Louvain, de Duve Institute and WELBIO, Brussels, Belgium.

Published: February 2019

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http://dx.doi.org/10.1038/s41375-018-0356-x	DOI Listing

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