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Characterization of Deletions of the HBA and HBB Loci by Array Comparative Genomic Hybridization
Thalassemia is among the most common genetic diseases worldwide. α-Thalassemia is usually caused by deletion of one or more of the duplicated HBA genes on chromosome 16. In contrast, most β-thalassemia results from point mutations that decrease or eliminate expression of the HBB gene on chromosome 1...
में बचाया:
| में प्रकाशित: | J Mol Diagn |
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| मुख्य लेखकों: | , , , , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
American Society for Investigative Pathology
2016
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4715224/ https://ncbi.nlm.nih.gov/pubmed/26612711 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jmoldx.2015.07.011 |
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