Hereditary spherocytosis (HS) due to loss of anion exchange transporter. [electronic resource]
Producer: 19930325Description: 450-6 p. digitalISSN:- 0390-6078
- Adult
- Anion Exchange Protein 1, Erythrocyte -- deficiency
- Blood Protein Electrophoresis
- Child
- Erythrocyte Aging
- Erythrocyte Deformability
- Female
- Genes, Dominant
- Glucosephosphate Dehydrogenase Deficiency -- complications
- Heterozygote
- Humans
- Male
- Spectrin -- analysis
- Spherocytes -- metabolism
- Spherocytosis, Hereditary -- blood
- Sulfates -- blood
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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