Author:
Hasanoglu Alev,Balwani Manisha,Kasapkara Çiğdem S.,Ezgü Fatih S.,Okur İlyas,Tümer Leyla,Çakmak Alpay,Nazarenko Irina,Yu Chunli,Clavero Sonia,Bishop David F.,Desnick Robert J.
Subject
Genetics(clinical),Genetics
Reference14 articles.
1. Anderson KE, Sassa S, Bishop DF, Desnick RJ (2001) Disorders of heme biosynthesis: X- linked sideroblastic anemia and the porphyrias. In: Scriver CR, Beaudet A, Sly WS, Valle D (eds) The metabolic and molecular basis of inherited diseases. McGraw-Hill, New York, pp 2991–3062
2. Berger H, Goldberg A (1955) Hereditary coproporphyria. Br Med J 2:85–88
3. Delfau-Larue MH, Martasek P, Grandchamp B (1994) Coproporphyrinogen oxidase: gene organization and description of a mutation leading to exon 6 skipping. Hum Mol Genet 3:1325–1330
4. Doss MO, Gross U, Lamoril J et al (1999) Compound heterozygous hereditary coproporphyria with fluorescing teeth. Ann Clin Biochem 36:680–682
5. Grandchamp B, Phung N, Nordmann Y (1977) Homozygous case of hereditary coproporphyria. Lancet 2:1348–1349
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