Publications by authors named "Wei-Xi Yuan"
Article Synopsis
- Thalassemia is the most prevalent genetic disorder globally, where identifying mutations is crucial for proper diagnosis and management.
- Standard tests often miss rare mutations, creating challenges for clinical labs in accurately diagnosing patients.
- A case study revealed a novel 71.8kb deletion affecting crucial genes responsible for α-thalassemia, leading to a proposed procedure for better identifying unusual mutations in thalassemia patients.
