Sökning: WFRF:(De Waele J. J.) > Characterization of...
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000 | 05500naa a2201873 4500 | |
001 | oai:prod.swepub.kib.ki.se:130658997 | |
003 | SwePub | |
008 | 240701s2015 | |||||||||||000 ||eng| | |
024 | 7 | a http://kipublications.ki.se/Default.aspx?queryparsed=id:1306589972 URI |
024 | 7 | a https://doi.org/10.1002/ajmg.a.368872 DOI |
040 | a (SwePub)ki | |
041 | a eng | |
042 | 9 SwePub | |
072 | 7 | a ref2 swepub-contenttype |
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100 | 1 | a Crow, YJ4 aut |
245 | 1 0 | a Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1 |
264 | c 2015-01-16 | |
264 | 1 | b Wiley,c 2015 |
700 | 1 | a Chase, DS4 aut |
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710 | 2 | a Karolinska Institutet4 org |
773 | 0 | t American journal of medical genetics. Part Ad : Wileyg 167167A:2, s. 296-312q 167167A:2<296-312x 1552-4833x 1552-4825 |
856 | 4 | u https://europepmc.org/articles/pmc4382202?pdf=render |
856 | 4 8 | u http://kipublications.ki.se/Default.aspx?queryparsed=id:130658997 |
856 | 4 8 | u https://doi.org/10.1002/ajmg.a.36887 |
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