Direct detection of point mutations by mismatch analysis: application to haemophilia B.
Rapid detection of point mutations in genomic DNA has been achieved by chemical mismatch analysis of heteroduplexes formed between amplified wild-type and target sequences in the human factor IX gene. Amplification and mismatch detection (AMD) analysis of DNA from relatives of haemophilia B patients...
में बचाया:
| में प्रकाशित: | Nucleic Acids Res |
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| मुख्य लेखकों: | , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Oxford University Press
1989
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| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC317779/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2726481/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/17.9.3347 |
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