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hereditary spherocytosis
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Summary
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Genetic Markers
Most Correlated Genes
Most Correlated SNPs
EPB42
SPTB
SLC4A1
SPTA1
ANK1
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Pathway Enrichment
Most Correlated Biogroups
STEINER_ERYTHROCYTE_MEMBRANE_GENES
GNF2_TAL1
GNF2_PCAF
GNF2_CDC27
GNF2_BNIP3L
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Curated Studies
Most Correlated Studies
TK6 cells treated with various clastogens, aneugens and formaldehyde
B lymphoblast TK6 cells treated with 15 genotoxic carcinogens
Mouse Phenotypes - Hereditary spherocytosis
Methylmethane Sulfonate ILSI-HESI Genotoxicity Study - human TK6 cell line subset
Carcinogen-induced changes in gene expression in TK6 lymphoblastoid cells
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Literature
Most Relevant Literature
Splenectomy in children with "mild" hereditary spherocytosis.
Comprehensive identification of erythrocyte membrane protein deficiency by 2D gel electrophoresis ba…
A case of hereditary spherocytosis misdiagnosed as pyruvate kinase deficient hemolytic anemia.
Use of capillary blood to diagnose hereditary spherocytosis.
Marked changes in red cell membrane proteins in hereditary spherocytosis: a proteomics approach.
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Clinical Trials
Most Relevant Clinical Trials
Hereditary Spherocytosis and Vascular Function
The Dallas Hereditary Spherocytosis Cohort Study
Hemolysis in Patients With Hereditary Spherocytosis (HS)
GDF 15 in Sickle Cell Disease and Hereditary Spherocytosis
Parvovirus B19 Infection in Hereditary Hemolytic Anemias Patients
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