Associated Papers
Biallelic variants in FLII cause pediatric cardiomyopathy by disrupting cardiomyocyte cell adhesion and myofibril organization.
Ruijmbeek CW et al.
Jci Insight, 2023
A human FLII gene variant alters sarcomeric actin thin filament length and predisposes to cardiomyopathy.
Kuwabara Y et al.
Proceedings of the National Academy of Sciences of the United States of America, 2023
37126682 (PubMed )
Supplement: pnas.2213696120.sapp.pdf
Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies.
Lipov A et al.
Nature Cardiovascular Research, 2023
38666070 (PubMed )
Supplement: 44161_2023_346_MOESM1_ESM.pdf
Categorized Genetic Analysis in Childhood-Onset Cardiomyopathy.
Al-Hassnan ZN et al.
Circulation. Genomic and Precision Medicine, 2020
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