A case of congenital fiber-type disproportion syndrome presenting dilated cardiomyopathy with ACTA1 mutation.
Matsumoto A, Tsuda H, Furui S, Kawada-Nagashima M, Anzai T, Seki M, Watanabe K, Muramatsu K, Osaka H, Iwamoto S, Nishino I, Yamagata T.
Matsumoto A, et al. Among authors: furui s.
Mol Genet Genomic Med. 2022 Sep;10(9):e2008. doi: 10.1002/mgg3.2008. Epub 2022 Jun 27.
Mol Genet Genomic Med. 2022.
PMID: 35757965
Free PMC article.