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- W2409959614 abstract "In this issue of Blood , 2 independent reports by [Rapetti-Mauss et al][1] and [Glogowska et al][2] describe the first example of a human disease: a novel type of hemolytic hereditary xerocytosis (HX) that is caused by a genetic defect in the Gardos channel, a Ca2+-sensitive K+ channel critical for" @default.
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- W2409959614 date "2015-09-10" @default.
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- W2409959614 title "More than one way to shrink" @default.
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- W2409959614 doi "https://doi.org/10.1182/blood-2015-07-657916" @default.
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