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1. Inherited human Apollo deficiency causes severe bone marrow failure and developmental defects

2. EFL1 mutations impair eIF6 release to cause Shwachman-Diamond syndrome

3. An in vivo genetic reversion highlights the crucial role of Myb-Like, SWIRM, and MPN domains 1 (MYSM1) in human hematopoiesis and lymphocyte differentiation

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