| Hb F-Cincinnati | Ggamma41(C7)Phe->Ser |
|---|
| ELECTROPHORESIS | Hb FX did not separate from Hb F at alkaline pH | ||
| IEF | Hb FX did not separate from Hb F by IEF | ||
| CHROMATOGRAPHY | Not reported | ||
| CHAIN SEPARATION | GgammaX = 29.5%; Ggamma = 37%; Agamma = 33.5% | ||
| STRUCTURE STUDIES | Tryptic digestion of gammaX chain; separation of peptides by reversed phase HPLC; amino acid analysis | ||
| DNA ANALYSES | A TTC->TCC mutation at codon 41 | ||
| NOTES | Found in a Caucasian newborn with cyanosis; baby became normal when Hb F disappeared after birth |
| REFERENCES | |||
| 1. | Kholi-Kumar, M., Zwerdling, T., and Rucknagel, D.L.: Am. J. Hematol., 49:43, 1995. | ||