Symptomatic Erythrocytosis Associated with a Compound Heterozygosity for Hb Lepore-Boston-Washington (δ87-β116) and Hb Johnstown [β109(G11)Val→Leu,GTG>TTG]-Reference-Cited by-同舟云学术

Symptomatic Erythrocytosis Associated with a Compound Heterozygosity for Hb Lepore-Boston-Washington (δ87-β116) and Hb Johnstown [β109(G11)Val→Leu,GTG>TTG]

Published:2012-05-07 Issue:4 Volume:36 Page:362-370
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Inoue Susumu,Oliveira Jennifer L.,Hoyer James D.,Sharman Mahesh

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2012.679717

Reference14 articles.

1. A New Electrophoretically Silent Variant That Causes Erythrocytosis

2. Hemoglobins with High Oxygen Affinity Leading to Erythrocytosis. New Variants and New Concepts

3. Hb Johnstown [?109 (G11) Val?Leu]: Second case described and associated for the first time with ?0-thalassemia in two Spanish families

4. The high oxygen-affinity Hemoglobin Johnstown [(β109(G11) Val→Leu] in a German kindred with an elevated erythrocyte hemoglobin content: Potential interaction with HFE mutations

5. Hb Johnstown [β109(G11)Val→Leu]: a High Oxygen Affinity Variant Associated with β0‐Thalassemia

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