Involvement of mitochondrial dysfunction in pathogenesis of hemophagocytic lymphohistiocytosis
Background: Hemophagocytic lymphohistiocytosis (HLH) is a hyper-inflammatory condition resulting from altered crosstalk between innate and adaptive immune responses. Familial HLH is caused by mutations in several genes whereas the acquired form is associated with infections, rheumatic diseases, mali...
Main Authors: | , , , , , |
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Format: | Article |
Language: | English |
Published: |
Discover STM Publishing Ltd
2019-06-01
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Series: | Journal of Biochemical and Clinical Genetics |
Subjects: | |
Online Access: | http://www.ejmanager.com/fulltextpdf.php?mno=18963 |