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High Throughput Molecular Confirmation of β-Thalassemia Mutations Using Novel TaqMan Probes
β-Thalassemia is a public health problem where 4.5% of Malaysians are β-thalassemia carriers. The genetic disorder is caused by defects in the β-globin gene complex which lead to reduced or complete absence of β-globin chain synthesis. Five TaqMan genotyping assays were designed and developed to det...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Molecular Diversity Preservation International (MDPI)
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3649372/ https://ncbi.nlm.nih.gov/pubmed/23429513 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/s130202506 |
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