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Whole-exome sequencing of a patient with severe and complex hemostatic abnormalities reveals a possible contributing frameshift mutation in C3AR1
Leinøe, Eva, Nielsen, Ove Juul, Jønson, Lars, Rossing, MariaVolume:
2
Language:
english
Journal:
Molecular Case Studies
DOI:
10.1101/mcs.a000828
Date:
July, 2016
File:
PDF, 864 KB
english, 2016