The molecular basis of the uroporphyrinogen III synthase (UROIIIS) deficiency was investigated in a member of a Japanese family. This defect in heme biosynthesis is responsible for a rare autosomal recessive disease: congenital erythropoietic porphyria (CEP) or Gu Β¨nther's disease. The patient was h
β¦ LIBER β¦
The identification and characterisation of alleles of sucrose phosphate synthase gene family III in sugarcane
β Scribed by C.L. McIntyre; M. Jackson; G.M. Cordeiro; O. Amouyal; S. Hermann; K.S. Aitken; F. Eliott; R.J. Henry; R.E. Casu; G.D. Bonnett
- Publisher
- Springer Netherlands
- Year
- 2006
- Tongue
- English
- Weight
- 243 KB
- Volume
- 18
- Category
- Article
- ISSN
- 1380-3743
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