A Splice Site Mutation Associated with Congenital CD59 Deficiency
Congenital CD59 deficiency is a recently described rare autosomal recessive disease associated with <i>CD59</i> gene mutations that lead to deficient or dysfunctional CD59 protein on the cell surface. The disease is characterized by the early onset of chronic hemolysis, relapsing periphe...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2022-05-01
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| Series: | Hematology Reports |
| Subjects: | |
| Online Access: | https://www.mdpi.com/2038-8330/14/2/25 |