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When both parents are carriers of the Beta Thalassemia trait, there is a 25% chance that every offspring will present with homozygous Beta Thalassemia Major with transfusion dependency

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(Its not clear if the peptides were responsible for the symptoms.) Considering the skin-darkening peptide melanotan II (sometimes called the Barbie peptide)

This is crucial for healing, as new vessels supply oxygen, nutrients, and reparative cells to damaged tissue