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Deficiencies in CBS activity caused by CBS genetic mutations are the most frequent cause of familial high homocysteine and the underlying cause of the homozygous CBS genetic disorder homocystinuria, which is characterized by severe high homocysteine levels

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Association study of 10 genes encoding neurotrophic factors and their receptors in adult and child attention-deficit/hyperactivity disorder

Chronic alcohol use damages hepatocytes and reduces phase II conjugation capacity

They may also recommend preventive care, such as safe immunizations for people with autoimmune diseases

It stimulates the secretion of HGH within the pituitary gland