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Heterozygous versus hemizygous (or homozygous) G6PD deficiency As the G6PD gene is on the X chromosome, males have only one allele, and if this has a mutation causing G6PD deficiency all the red cells will be G6PD deficient

Compared to healthy individuals, MS patients, both with and without calciphylaxis, exhibit elevated basal expression levels of hypoxia-related proteins (GLUT1 and VEGF), with the highest levels observed in those with calciphylaxis (182)