Rare ?-thalassemia mutations are cause of concern
Open Access
- 22 June 2004
- journal article
- Published by Wiley in American Journal of Hematology
- Vol. 76 (3) , 312
- https://doi.org/10.1002/ajh.20084
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Initiation codon mutation in an Asian Indian familyAmerican Journal of Hematology, 2002
- A NOVEL β0-THALASSEMIA MUTATION AT CODON 55 (−A) AND A RARE 17 bp DELETION AT CODONS 126–131 IN THE INDIAN POPULATIONHemoglobin, 2002
- The same “TATA” box β-thalassemia mutation in Chinese and US blacks: another example of independent origins of mutationHuman Genetics, 1986
- beta-Thalassemia in American Blacks: novel mutations in the "TATA" box and an acceptor splice site.Proceedings of the National Academy of Sciences, 1984