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what r porphyrias?
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Answer / bhanu
they are inherited and acquired disorders caused by a
deficiency of an enzyme in the hame biosynthetic
pathway.about 15% occurs in the liver and remaining in
erythrocyte precursors. porpyrias are of two types. hepatic
and erythropoietic types.they are erythropoietic
porphyria,acute intermittent porphyria,heriditary
porphyria,cutanea tarda,and lead poisoning.
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I understand that urine can act as a reagent to break disulfide bonds? I am particularly interested in bonds between cysteines. and or any other amino acids.
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