Decoding hereditary spherocytosis: Unveiling the genes as a potential causative agent
Hereditary spherocytosis (HS) is the most common inherited hemolytic anemia in populations of northern European descent, arising from mutations in genes encoding key erythrocyte membrane proteins, including ANK1, SPTB, SLC4A1, SPTA1, and EPB42. These genetic defects disrupt the vertical linkages bet...
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| Asıl Yazarlar: | , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Wolters Kluwer Medknow Publications
2026-01-01
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| Seri Bilgileri: | Iraqi Journal of Hematology |
| Konular: | |
| Online Erişim: | https://journals.lww.com/10.4103/ijh.ijh_134_25 |
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