Characterization of human disease phenotypes associated with mutations in <i>TREX1</i>, <i>RNASEH2A</i>, <i>RNASEH2B</i>, <i>RNASEH2C</i>, <i>SAMHD1</i>, <i>ADAR</i>, and <i>IFIH1</i>Yanick J. Crow, Corinne De Laet, Johanna L. Schmidt et al.|American Journal of Medical Genetics Part A|2015Cited by 617