Publication Cover
Hemoglobin
international journal for hemoglobin research
Volume 13, 1989 - Issue 5
11
Views
9
CrossRef citations to date
0
Altmetric
Original Article

HB Bruxelles: α2Aβ241 or 42(C7 or CD1) Phe Deleted

, , , , , , & show all
Pages 465-474 | Received 21 Mar 1988, Accepted 28 Mar 1989, Published online: 07 Jul 2009
 

Abstract

Hb Bruxelles is a new β-globin variant producing severe congenital Heinz body anemia. It results from the deletion of one of the two adjacent phenylalanines, β41 or β42, presumably by frameshift mutagenesis. Its whole blood oxygen affinity is significantly lowered.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.