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Yu H, Rao X, Zhang K
Rather than being investigated within a single biological pathway, it has featured in laboratory studies examining molecular signalling, extracellular matrix biology and the complex interactions that influence normal tissue organisation
The inheritance of G6PD deficiency is clinically classified as an X-linked recessive disorder, however, because heterozygous females can develop hemolytic episodes the disorder is not truly recessive in the Mendelian sense
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