Gene deletions in alpha thalassemia prove that the 5' zeta locus is functional.

The deletions in the zeta-alpha globin gene cluster in two infants with the hemoglobin Bart's hydrops fetalis syndrome (homozygous alpha thalassemia 1) have been mapped by restriction endonuclease analysis using a zeta-specific probe. DNA from a Thai infant lacked the psi alpha 1 gene and both alpha...

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Detalhes bibliográficos

Publicado no:	Proc Natl Acad Sci U S A
Principais autores:	Pressley, L, Higgs, D R, Clegg, J B, Weatherall, D J
Formato:	Artigo
Idioma:	Inglês
Publicado em:	National Academy of Sciences 1980
Assuntos:	Research Article
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC349662/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6158051/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.77.6.3586
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