Hb ananosa or α2111(G18)Ala → Valβ (α2 Mutation) and Hb mulhacen or α2123(H6)Ala → Serβ2 (αl Mutation) are two silent stable variants detected by sequencing of amplified dna
E. G. Kazanetz, T. H. J. Huisman(Johannes Gutenberg University Mainz), J.Ye. Leonova(Augusta University), J. B. Wilson, J. Mi. de Pablos Gallego(Hospital Universitario Virgen de las Nieves), M. Walbrecht, S. K. McMillan
Cited by 2
Related Papers
Endothelin-1 decreases glutamate uptake in primary cultured rat astrocytes
|American Journal of Physiology-Cell Physiology|2001|48
Variability in the fetal hemoglobin level of the normal adult
|American Journal of Hematology|1996|40
Hb lulu island (α<sub>2</sub>β<sub>2</sub>107[G9]Gly→Asp)‐β°‐thalassemia (codon 15; TGG → TAG), a form of thalassemia intermedia
|American Journal of Hematology|1995|16
Co-Inheritance of Hb D-PUNJAB (CODON 121; GAA→CAA) and β0-Thalassemia (IVS-II-1; G→A)
|Journal of Pediatric Hematology/Oncology|1996|16
The αβ- andα2α1-globin mRNA ratios in different forms of α-thalassemia
|Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease|1996|15