Human Genome Epidemiology Literature Finder
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Query Trace: Syndrome and KLRC3[original query] |
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Whole-exome sequencing of sickle cell disease patients with hyperhemolysis syndrome suggests a role for rare variation in disease predisposition. Transfusion 2017 Dec . Mwesigwa Savannah, Moulds Joann M, Chen Alice, Flanagan Jonathan, Sheehan Vivien A, George Alex, Hanchard Neil |
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- Page last updated:Apr 22, 2024
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