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TABLE 2 Comparison of the Two Most Common Variants of G6PD Deficiency Diagnosis The diagnosis of G6PD deficiency is made by a quantitative spectrophotometric analysis or, more commonly, by a rapid fluorescent spot test detecting the generation of NADPH from NADP
Bomba M, Ciavardelli D, Silvestri E, Canzoniero LM, Lattanzio R, Chiappini P, et al
The entire process of mitochondrial fusion can be briefly summarized as mitochondrial trans-bolus, mitochondrial outer membrane fusion, and mitochondrial inner membrane fusion (Lee H
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