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Abstract
Genetic variant spectrum in 265 Chinese patients with hemophagocytic lymphohistiocytosis: molecular analyses of <i>PRF1</i> , <i>UNC13D</i> , <i>STX11</i> , <i>STXBP2</i> , <i>SH2D1A</i> , and <i>XIAP</i>
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