Advanced search
Publication Cover
Hemoglobin
international journal for hemoglobin research
Volume 26, 2002 - Issue 4
Submit an article Journal homepage
39
Views
5
CrossRef citations to date
0
Altmetric
Original

Hb MANAWATU [α37(C2)Pro→Leu]: A NEW MILDLY UNSTABLE MUTATION AT AN INVARIANT PROLINE RESIDUE

Stephen O. Brennan Molecular Pathology Laboratory, Canterbury Health Laboratories, P.O. Box 151, Christchurch, New Zealand
,
Campbell Sheen Molecular Pathology Laboratory, Canterbury Health Laboratories, P.O. Box 151, Christchurch, New Zealand
&
Stephen Johnson Haematology Laboratory, Medlab Central, Palmerston North Hospital, Palmerston North, New Zealand
Pages 389-392 | Received 14 Jun 2002, Accepted 21 Jun 2002, Published online: 07 Jul 2009

Citations (5)

Keep up to date with the latest research on this topic with citation updates for this article.

Subscribe to citation updates

Read on this site (3)

Agathe Horri-Naceur & David J. Timson. (2020) In Silico Analysis of the Effects of Point Mutations on α-Globin: Implications for α-Thalassemia. Hemoglobin 44:2, pages 89-103.
Read now
Florens G.A. Versteegh, Sandra G.J. Arkesteijn, Margreet Bakker-Verweij, Karola Haanappel, Peter van Delft, Marion Phylipsen, Judith O. Kaufmann, Peter J.M.J. Kok, Gideon W.A. Lansbergen, Piero C. Giordano & Cornelis L. Harteveld. (2011) Hb Boskoop [HBA2c.112C>T p.Pro38Ser]: A New α2 Chain Variant Observed in a Morrocan Family. Hemoglobin 35:2, pages 97-102.
Read now
Varvara Douna, Ioannis Papassotiriou, Anna Metaxotou-Mavrommati, Alexandra Stamoulakatou, Dimitra Liapi, Dimitrios Kampourakis, Amalia Tsilimigaki, Emmanuel Kanavakis & Joanne Traeger-Synodinos. (2008) Further Identification of The Hyperunstable α-Globin Chain Variant Hb Heraklion [codons 36/37 (–CCC); Pro→0 (α1)] in Greek Cases With Co-Inherited α+-Thalassemia Mutations. Hemoglobin 32:4, pages 379-385.
Read now

Articles from other publishers (2)

Todd L. Mollan, Bindu Abraham, Michael Brad Strader, Yiping Jia, Jay N. Lozier, John S. Olson & Abdu I. Alayash. (2012) Familial secondary erythrocytosis due to increased oxygen affinity is caused by destabilization of the T state of hemoglobin Brigham (α 2 β 2 Pro100Leu ) . Protein Science 21:10, pages 1444-1455.
Crossref
Stephen O Brennan. (2008) Fifty-Eight Years of Hemoglobin Analysis. Clinical Chemistry 54:1, pages 8-10.
Crossref

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:

Order Reprints Request Corporate Permissions

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:

Request Academic Permissions

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.

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.