One form of inclusion body beta-thalassemia is due to a GAA----TAA mutation at codon 121 of the beta chain.

Y. J. Fei, T. A. Stoming, A. Kutlar, T. H. Huisman, G. Stamatoyannopoulos

Research output: Contribution to journalLetterpeer-review

47 Scopus citations

Fingerprint

Dive into the research topics of 'One form of inclusion body beta-thalassemia is due to a GAA----TAA mutation at codon 121 of the beta chain.'. Together they form a unique fingerprint.