A large deletion in the human alpha-globin cluster caused by a replication error is associated with an unexpectedly mild phenotype.
We have characterized a newly identified 16.6 kb deletion which removes a significant proportion of the human alpha-globin cluster including the psizeta1, alpha(D), psialpha1 and alpha2-globin genes but leaves the duplicated alpha1 gene intact. This complicated rearrangement results from a combinati...
Những tác giả chính: | Rugless, M, Fisher, C, Old, J, Sloane-Stanley, J, Ayyub, H, Higgs, D, Garrick, D |
---|---|
Định dạng: | Journal article |
Ngôn ngữ: | English |
Được phát hành: |
2008
|
Những quyển sách tương tự
-
A 16.5 kb deletion in the alpha globin cluster associated with an extremely mild phenotype
Bằng: Rugless, M, et al.
Được phát hành: (2007) -
Deletion of the mouse alpha-globin regulatory element (HS -26) has an unexpectedly mild phenotype.
Bằng: Anguita, E, et al.
Được phát hành: (2002) -
Deletion of the mouse alpha globin regulatory element (HS-26) has an unexpectedly mild phenotype.
Bằng: Anguita, E, et al.
Được phát hành: (2003) -
The role of the polycomb complex in silencing alpha-globin gene expression in nonerythroid cells.
Bằng: Garrick, D, et al.
Được phát hành: (2008) -
A novel deletion causing alpha thalassemia clarifies the importance of the major human alpha globin regulatory element.
Bằng: Viprakasit, V, et al.
Được phát hành: (2006)