## Communicated by Peter Oefner Beta-thalassemia is a common inherited disease, resulting from one or more of a total of more than 200 different mutations in the b-globin gene (HBB). Efficient and reliable mutation-screening methods are essential in order to establish appropriate prevention program
Rapid mutation detection in complex genes by heteroduplex analysis with capillary array electrophoresis
✍ Scribed by Eladio Velasco; Mar Infante; Mercedes Durán; Eva Esteban-Cardeñosa; Enrique Lastra; Carlos García-Girón; Cristina Miner
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 346 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0173-0835
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