Article

Reversible Mitochondrial Fragmentation in iPSC-Derived Cardiomyocytes from Children with DCMA, a Mitochondrial Cardiomyopathy

2019-08-12

Abstract excerpt

<h4>ABSTRACT</h4> <h4>Background</h4> The dilated cardiomyopathy with ataxia syndrome (DCMA) is an understudied autosomal recessive disease caused by loss-of-function mutations in the poorly characterized gene DNAJC19 . Clinically, DCMA is commonly associated with heart failure and early death in affected children through an unknown mechanism. DCMA has been linked to Barth syndrome, a rare but well-studied diso...

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Literature Corpus work: 54e9fc36-1fa4-5db6-ba25-d3ad0a64e165
DOI: 10.1101/732339

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