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Description
Sanger sequencing is widely applied to identify disease-causing mutations in cases where traditional testing has failed or when a patient has been extensively transfused, leading to confounding biochemical and other testing findings due to mixed RBC populations
SCFAs, Short-chain fatty acids (butyrate, acetate, propionate)
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In a recent report, Yue et al
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doi:10.1021/jo01151a027
