Correlations With Point Mutations and Severity of Hemolitic Anemias: The Example of Hereditary Persistence of Fetal Hemoglobin With Sickle Cell Anemia and Beta Thalassemia

doi 10.5772/36240
Full Text
Abstract

Available in full text

Date
Authors
Publisher

InTech

Related search

Hereditary Persistence of Fetal Hemoglobin-Beta-Thalassemia Syndrome

2020English

Hereditary Persistence of Fetal Hemoglobin-Sickle Cell Disease Syndrome

2020English

Hydroxyurea Enhances Fetal Hemoglobin Production in Sickle Cell Anemia.

Journal of Clinical Investigation
Medicine
1984English

Nuclear Proteins That Bind the Human Gamma-Globin Gene Promoter: Alterations in Binding Produced by Point Mutations Associated With Hereditary Persistence of Fetal Hemoglobin.

Molecular and Cellular Biology
Cell BiologyMolecular Biology
1988English

DNA Methylation in Hereditary Persistence of Fetal Hemoglobin (HPFH-2)

Nucleic Acids Research
Genetics
1987English

Sickle Beta+ Thalassemia

Chettinad Health City Medical Journal
2014English

Role of Extracellular Hemoglobin in Thrombosis and Vascular Occlusion in Patients With Sickle Cell Anemia

Anemia
HematologyCell Biology
2011English

Molecular Epidemiology and Hematologic Characterization of Δβ-Thalassemia and Hereditary Persistence of Fetal Hemoglobin in 125,661 Families of Greater Guangzhou Area, the Metropolis of Southern China

BMC Medical Genetics
Genetics
2020English

Health-Related Quality of Life Is Associated With Hemoglobin Level in Children With Sickle Cell Anemia

Journal of Blood Disorders & Transfusion
2012English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy