Whole-Exome Sequencing Reveals Mutations in Genes Linked to Hemophagocytic Lymphohistiocytosis and Macrophage Activation Syndrome in Fatal Cases of H1N1 Influenza.

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Published in J Infect Dis on November 23, 2015

Authors

Grant S Schulert1, Mingce Zhang2, Ndate Fall1, Ammar Husami3, Diane Kissell3, Andrew Hanosh4, Kejian Zhang3, Kristina Davis4, Jeffrey M Jentzen4, Lena Napolitano5, Javed Siddiqui6, Lauren B Smith4, Paul W Harms7, Alexei A Grom1, Randy Q Cron2

Author Affiliations

1: Division of Pediatric Rheumatology, Cincinnati Children's Hospital Medical Center, Ohio.
2: Division of Pediatric Rheumatology, Children's Hospital of Alabama/University of Alabama at Birmingham.
3: Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Ohio.
4: Department of Pathology, University of Michigan Medical School, Ann Arbor.
5: Department of Surgery, University of Michigan Medical School, Ann Arbor.
6: Department of Pathology, University of Michigan Medical School, Ann Arbor Michigan Center for Translational Pathology, University of Michigan Medical School, Ann Arbor.
7: Department of Pathology, University of Michigan Medical School, Ann Arbor Department of Dermatology, University of Michigan Medical School, Ann Arbor Michigan Center for Translational Pathology, University of Michigan Medical School, Ann Arbor.

Associated clinical trials:

Rutgers COVID-19 Cohort Study | NCT04336215

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