Mitapivat reprograms the RBC metabolome and improves anemia in a mouse model of hereditary spherocytosis
Author:
Funder
Agios Pharmaceuticals, Inc.
MIUR
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Link
https://insight.jci.org/articles/view/172656/files/pdf
Reference58 articles.
1. Advances in understanding the pathogenesis of red cell membrane disorders
2. Hereditary spherocytosis
3. Genetics and Genomics Approaches for Diagnosis and Research Into Hereditary Anemias
4. Metabolic Fingerprint in Hereditary Spherocytosis Correlates With Red Blood Cell Characteristics and Clinical Severity
5. Membrane cation and anion transport activities in erythrocytes of hereditary spherocytosis: Effects of different membrane protein defects
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