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...

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Detalhes bibliográficos

Publicado no:	Nucleic Acids Res
Principais autores:	Montandon, A J, Green, P M, Giannelli, F, Bentley, D R
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Oxford University Press 1989
Acesso em linha:	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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