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Rapid diagnosis of spinal muscular atrophy using High-Resolution Melting Analysis
BACKGROUND: Spinal muscular atrophy (SMA) is an autosomal recessive hereditary disorder caused by mutations of the survival motor neuron 1 (SMN1) gene. Recently, high-resolution DNA melting analysis (HRMA) with saturation LC Green dyes has become a powerful post-PCR technique for genotyping or mutat...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2694785/ https://ncbi.nlm.nih.gov/pubmed/19480685 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-10-45 |
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