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

T. W. Kang, S. W. Oh, M. R. Kim, Js Lee, S. C. Kim

Research output: Contribution to journalLetterpeer-review

4 Citations (Scopus)

Fingerprint

Dive into the research topics of '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'. Together they form a unique fingerprint.