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January 1, 1998Human Mutation

Fluorescent chemical cleavage of mismatches for efficient screening of the factor VIII gene

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Authors

KFKathleen FresonKU LeuvenKPKathelijne PeerlinckKU LeuvenTATania AguirreCentre National de la Recherche Scientifique

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Cite This Study

Freson et al. (1998) studied this question.

synapsesocial.com/papers/6a87efb48dfe8b7ec5a52d9ehttps://doi.org/10.1002/(sici)1098-1004(1998)11:6<470::aid-humu8>3.0.co;2-a
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Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Molecular characterization of severe hemophilia A suggests that about half the mutations are not within the coding regions and splice junctions of the factor VIII gene.1991 · 158 citations
  2. 2The haemophilia A mutation search test and resource site, home page of the factor VIII mutation database: HAMSTeRS1996 · 31 citations
  3. 3Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms.1989 · 3,642 citations
  4. 4Reactivity of cytosine and thymine in single-base-pair mismatches with hydroxylamine and osmium tetroxide and its application to the study of mutations.1988 · 623 citations