A genetic combination of silent beta-thalassaemia, high Hb A2 beta-thalassaemia, and single alpha globin gene deletion causing mild thalassaemia intermedia.

This paper reports a Sardinian patient, who was a compound heterozygote for silent beta-thalassaemia and high Hb A2 beta o-thalassaemia with the clinical phenotype of mild thalassaemia intermedia; alpha globin gene mapping showed a single alpha globin gene deletion. The reduced alpha globin chain ou...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Galanello, R, Maccioni, L, Rosatelli, M C, Ibba, P, Nurchi, A M, Cao, A
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1984
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1049250/
https://ncbi.nlm.nih.gov/pubmed/6716419
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