abstract |
A method for detecting a mutation associated with a gene encoding OAS1 is provided. A human genetic screening method for identifying a mutation in an oligoadenylate synthetase gene (OAS1), the method comprising: dereferencing a reference nucleotide in a specific base sequence of a reference sequence Detecting a presence in the nucleic acid sample for the presence of an OAS1 point mutation selected from the group consisting of nucleotide substitutions, as well as deletions, thereby identifying the mutation. [Selection] Figure 5A |