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CORRESPONDENCE|
March 1, 1989
One form of inclusion body beta-thalassemia is due to a GAA----TAA mutation at codon 121 of the beta chain [letter]
Blood (1989) 73 (4): 1075–1077.
![First page of One form of inclusion body beta-thalassemia is due to a GAA----TAA mutation at codon 121 of the beta chain [letter]](https://ash.silverchair-cdn.com/ash/content_public/journal/blood/73/4/10.1182_blood.v73.4.1075.1075/1/1075.pdf.gif?Expires=1748020963&Signature=aRvCQH81nr129Kt4aZoYP3uuxtoHgVRcLB35~GpNUhmUSAzTos7-dbxPpyQ3iqpBiI--gFyAeLnz8lqqOUmY3WUwBNG-~gEuzuP6v0Py28mgnVM0~KOjLNUHAy7Fbd4~m0O8RM6SeUOQgK7K36y~VJmwP1xx0LfX9palgRZKzJXamVYRz~vzmmEA5j-qhet-GWLVfdnECY694j9h7epdb5Qkh3zS~g9kZ495zmLDB-Xoko7h5e01Uf3285cgGakIyo871gKBLuCg972dKhHbzz4koSKFQqvNj4yZ1a6~CNHWgKeoQNHCMK5YJuAqp4eLXmHYp7ySDiAk3hSHAVTiXg__&Key-Pair-Id=APKAIE5G5CRDK6RD3PGA)
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