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bpc 157 cas BPC-157, 5mg | Purity Peptides
Description
Genetics may affect the activity of enzymes involved in absorption, binding to B 12 blood transport or intracellular proteins and/or B 12 metabolism

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Severe cases of homocystinuria are typically caused by autosomal recessive genetic defects and exhibit characteristic clinical features including ocular lens dislocation, marfanoid features and other skeletal abnormalities including osteoporosis, intellectual disability, and thromboembolic disease, the latter frequently being the cause of premature death in affected individuals (28)
