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interferonopathies [PMID: 34671122]. Our group previously identified a type I interferonopathy associated with homozygous mutation of STAT2 [PMID: 31836668]. We have generated a mouse model of this disorder, in which
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develop experience in in vivo modelling, molecular profiling, and drug testing, with access to state-of-the-art facilities and expert support. You will also benefit from tailored training and mentoring, and
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