#160 : Detection of Alpha Thalassemia Silent Carriers Having Point Mutation Among Infertile Patients by Gene Sequencing
Background and Aims: Thalassemia is a highly prevalent genetic disease in Vietnam. Importantly, silent carriers pose a risk of having children with two mutated alleles hence serious health conditions requiring hematological treatments for the lifetime. Early detection of silent carriers would assist...
| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
World Scientific Publishing
2023-12-01
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| Series: | Fertility & Reproduction |
| Online Access: | https://www.worldscientific.com/doi/10.1142/S2661318223743497 |