Article
Compound heterozygosity for a premature termination codon and missense mutation in the exon 10 of the uroporphyrinogen III cosynthase gene causes a severe phenotype of congenital erythropoietic porphyria.
Journal of the European Academy of Dermatology and Venereology : JEADV - 1 Apr 2009
Kang T-W, Oh S-W, Kim M-R, Lee J S, Kim S-C
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