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coproporphyria
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CPOX
Expression of coproporphyrinogen oxidase and synthesis of hemoglobin in human erythroleukemia K562 cells
Characterization of mutations in the CPO gene in British patients demonstrates absence of genotype-phenotype correlation and identifies relationship between hereditary coproporphyria and harderoporphyria
Mutant and wild-type alpha-synuclein interact with mitochondrial cytochrome C oxidase
Two novel mutations and coexistence of the 991C>T and the 1339C>T mutation on a single allele in the coproporphyrinogen oxidase gene in Swedish patients with hereditary coproporphyria
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