Gene Deletion as the Molecular Basis for the Kenya-Gγ-Hpfh Condition-Reference-Cited by-同舟云学术

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Gene Deletion as the Molecular Basis for the Kenya-Gγ-Hpfh Condition

Published:1983-01 Issue:2 Volume:7 Page:115-123
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Ojwang P. J.,Nakatsuji T.,Gardiner M. B.,Reese A. L.,Gilman J. G.,Huisman T. H. J.

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630268309048641

Reference14 articles.

1. Hemoglobin Kenya, the product of fusion of γ and β polypeptide chains

3. The Kenya Form of Hereditary Persistence of Fetal Haemoglobin: Structural Studies and Evidence for Homogeneous Distribution of Haemoglobin F using Fluorescent Anti-haemoglobin F Antibodies

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1. Disrupting the adult globin promoter alleviates promoter competition and reactivates fetal globin gene expression;Blood;2022-04-07

2. Thalassemia Syndromes;Hematology;2018

3. Genome editing using CRISPR-Cas9 to create the HPFH genotype in HSPCs: An approach for treating sickle cell disease and β-thalassemia;Proceedings of the National Academy of Sciences;2016-09-06

4. Human Hemoglobin;Vogel and Motulsky's Human Genetics;2010

5. Epigenetics;Vogel and Motulsky's Human Genetics;2010

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