Article
Tafazzin regulates neutrophil maturation and inflammatory response
2024-06-05
Abstract excerpt
<h4>ABSTRACT</h4> Barth syndrome (BTHS) is a rare genetic disease caused by mutations in the TAFAZZIN gene. It is characterized by neutropenia, cardiomyopathy and skeletal myopathy. Neutropenia in BTHS is associated with life-threatening infections, yet there is little understanding of the molecular and physiological causes of this phenomenon. We combined bone marrow analysis, CRISPR/Cas9 genome editing in hematop...
Topics
Open a Topic to create a Post that cites this publication.
Identifiers and source
- Literature Corpus work
- bec89586-6768-5043-8c13-e112c577765f
- DOI
- 10.1101/2024.06.05.24307331
