Using CRISPR/CAS9 technology, a single nucleotide change was introduced into the Stat3 gene to create a knock-in mouse model harboring a de novo pathogenic human STAT3 variant (p.G421R). (J:331798)
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Using CRISPR/CAS9 technology, a single nucleotide change was introduced into the Stat3 gene to create a knock-in mouse model harboring a de novo pathogenic human STAT3 variant (p.G421R). (J:331798)