Reduction in mRNA Expression of the Neutrophil Chemoattract Factor CXCL1 in <i>Pseudomonas aeruginosa</i> Treated Barth Syndrome B Lymphoblasts
Barth Syndrome (BTHS) is a rare X-linked genetic disease caused by a mutation in the <i>TAFAZZIN</i> gene, which codes for the protein tafazzin involved in cardiolipin remodeling. Approximately 70% of patients with BTHS exhibit severe infections due to neutropenia. However, neutrophils f...
| Main Authors: | , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2023-05-01
|
| Series: | Biology |
| Subjects: | |
| Online Access: | https://www.mdpi.com/2079-7737/12/5/730 |