The effect of HBB: c.*+96T>C (3'UTR +1570 T>C) on the mild b-thalassemia intermedia phenotype

Hemoglobin beta (HBB): c.*+96T>C substitution is very rare among β-globin gene mutations and its clinical significance remains to be clarified. The present study aimed to investigate the role of HBB: c.*+96T>C in the β-thalassemia intermedia phenotype in a Turkish family. The proband and...

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Hlavní autoři:	Türker Bilgen, Duran Canatan, Yunus Arıkan, Akif Yeşilipek, İbrahim Keser
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Turkish Society of Hematology 2011-08-01
Edice:	Turkish Journal of Hematology
Témata:	mild β -thalassemia intermedia b-globin gene hbb: c.*+96t>c
On-line přístup:	https://jag.journalagent.com/z4/download_fulltext.asp?pdir=tjh&un=TJH-48742
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