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Autor:
Jessika B. Iwanski, Christopher T. Pappas, Rachel M. Mayfield, Gerrie P. Farman, Rebecca Ahrens-Nicklas, Jared M. Churko, Carol C. Gregorio
Publikováno v:
npj Regenerative Medicine, Vol 9, Iss 1, Pp 1-21 (2024)
Abstract Neonatal dilated cardiomyopathy (DCM) is a poorly understood muscular disease of the heart. Several homozygous biallelic variants in LMOD2, the gene encoding the actin-binding protein Leiomodin 2, have been identified to result in severe DCM
Externí odkaz:
https://doaj.org/article/d3e3b84a14fb40d49e229be1589d0e31