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HARVARD Citation
Poulain, S. et al. (n.d.). MYD88 L265P mutation contributes to the diagnosis of Bing Neel syndrome. British journal of haematology. pp. 506-513. [Online].
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Poulain, S. et al. (n.d.). MYD88 L265P mutation contributes to the diagnosis of Bing Neel syndrome. British journal of haematology. pp. 506-513. [Online].