Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1
Identifiers
Identifiers
URI: http://hdl.handle.net/20.500.11940/4352
PMID: 25604658
DOI: 10.1002/ajmg.a.36887
ISSN: 1552-4825
Date issued
2015Journal title
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
Type of content
Artigo