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Real World Application: G6PD Deficiency Disorder Deficiency in G6PD is a hereditary X-linked recessive disorder that mostly found in men, and frequently occurs in African Americans, Asians, and Mediterranean peoples
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In order to target roGFP2 into the periplasm, roGFP2 was PCR amplified using the primer pair listed in Supplementary Table S3 from the pCC_ roGFP2 plasmid as template
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