A Kindred with a β-Globin Base Substitution [β89(F5)Ser→Arg (AGT>AGG); HBB: c.270T>G] Resulting in Hemoglobin Vanderbilt-Reference-Cited by-同舟云学术

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A Kindred with a β-Globin Base Substitution [β89(F5)Ser→Arg (AGT>AGG); HBB: c.270T>G] Resulting in Hemoglobin Vanderbilt

Published:2019-09-03 Issue:4-5 Volume:43 Page:273-276
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Shomali William¹^ORCID,Brar Rondeep¹,Arekapudi Subramanyeswara R.²,Gotlib Jason R.¹

Affiliation:

1. Division of Hematology, Stanford Cancer Institute, Stanford University School of Medicine, Stanford, CA, USA;

2. Division of Hematology and Oncology, VA Central California Health Care System/UCSF Fresno Center for Medical Education and Research, Fresno, CA, USA

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2019.1680382

Reference9 articles.

1. Oxygen Sensing, Homeostasis, and Disease

2. The Polycythemias

3. Polycythemia associated with a hemoglobinopathy.

4. Haemoglobin Vanderbilt (α2β289Ser→Arg): a New Haemoglobin with High Oxygen Affinity and Compensatory Erythrocytosis

5. A Novel Base Change Leading to Hb Vanderbilt [β89(F5)Ser→Arg, AGT>AGA]

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