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Because it is unusually stable in plasma and dissolves easily in solution, it is frequently chosen for studies focused on regeneration and recovery

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[5] Most people who develop symptoms are male, due to the X-linked pattern of inheritance, but female carriers can be affected due to unfavorable lyonization or skewed X-inactivation, where random inactivation of an X chromosome in certain cells creates a population of G6PD-deficient red blood cells coexisting with unaffected red blood cells