Stem cell models of TAFAZZIN deficiency reveal novel tissue-specific pathologies in Barth syndrome - PubMed Barth syndrome (BTHS) is a rare mitochondrial disease caused by pathogenic variants in the gene TAFAZZIN, which leads to abnormal cardiolipin (CL) metabolism on the inner mitochondrial membrane. Altho...

Check out the latest publication from my lab and the culmination of my wonderful graduate student, Olivia's, thesis work:
pubmed.ncbi.nlm.nih.gov/39535077/

Trying this out!