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Psoriatic plaques exhibit red autofluorescence that is due to protoporphyrin IX.

Detection of a R173W mutation in the porphobilinogen deaminase gene in the Nova Scotian "foreign Protestant" population with acute intermittent porphyria: a founder effect.

A molecular view of the neurologic porphyrias.

Environmental chemical exposures and disturbances of heme synthesis.

Hereditary coproporphyria: exon screening by heteroduplex analysis detects three novel mutations in the coproporphyrinogen oxidase gene.

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