De novo deletion within the telomeric region flanking the human alpha globin locus as a cause of alpha thalassaemia.
We have identified and characterized a Scottish individual with alpha thalassaemia, resulting from a de novo 48 kilobase (kb) deletion from the telomeric flanking region of the alpha globin cluster which occurred as a result of recombination between two misaligned repetitive elements that normally l...
Main Authors: | Viprakasit, V, Kidd, A, Ayyub, H, Horsley, S, Hughes, J, Higgs, D |
---|---|
Format: | Journal article |
Language: | English |
Published: |
2003
|
Similar Items
-
A novel deletion causing alpha thalassemia clarifies the importance of the major human alpha globin regulatory element.
by: Viprakasit, V, et al.
Published: (2006) -
Hb H hydrops fetalis syndrome associated with the interaction of two common determinants of alpha thalassaemia (--MED/(alpha)TSaudi(alpha)).
by: Viprakasit, V, et al.
Published: (2002) -
Deletion of the alpha-globin gene cluster as a cause of acquired alpha-thalassemia in myelodysplastic syndrome.
by: Steensma, D, et al.
Published: (2004) -
The mouse alpha-globin locus regulatory element.
by: Gourdon, G, et al.
Published: (1995) -
The alpha thalassaemias.
by: Higgs, D, et al.
Published: (2009)