Cargando…
Mutations in the paralogous human α-globin genes yielding identical hemoglobin variants
The human α-globin genes are paralogues, sharing a high degree of DNA sequence similarity and producing an identical α-globin chain. Over half of the α-globin structural variants reported to date are only characterized at the amino acid level. It is likely that a fraction of these variants, with phe...
Autores principales: | Moradkhani, Kamran, Préhu, Claude, Old, John, Henderson, Shirley, Balamitsa, Vera, Luo, Hong-Yuan, Poon, Man-Chiu, Chui, David H. K., Wajcman, Henri, Patrinos, George P. |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2008
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2690850/ https://www.ncbi.nlm.nih.gov/pubmed/18923834 http://dx.doi.org/10.1007/s00277-008-0624-3 |
Ejemplares similares
-
Abnormal haemoglobins: detection & characterization
por: Wajcman, Henri, et al.
Publicado: (2011) -
Role of α-Globin H Helix in the Building of Tetrameric Human Hemoglobin: Interaction with α-Hemoglobin Stabilizing Protein (AHSP) and Heme Molecule
por: Domingues-Hamdi, Elisa, et al.
Publicado: (2014) -
Updates of the HbVar database of human hemoglobin variants and thalassemia mutations
por: Giardine, Belinda, et al.
Publicado: (2014) -
Clinically relevant updates of the HbVar database of human hemoglobin variants and thalassemia mutations
por: Giardine, Belinda M, et al.
Publicado: (2020) -
GLOBIN UTILIZATION BY THE ANEMIC DOG TO FORM NEW HEMOGLOBIN
por: Robscheit-Robbins, F. S., et al.
Publicado: (1937)