Associated Papers
Human disease-causing mutations result in loss of leiomodin 2 through nonsense-mediated mRNA decay.
Pappas CT et al.
Plos Genetics, 2024
Whole-Exome Sequencing Identifies Homozygote Nonsense Variants in LMOD2 Gene Causing Infantile Dilated Cardiomyopathy.
Sono R et al.
Cells, 2023
Diagnostic yield of genetic testing in a multinational heterogeneous cohort of 2088 DCM patients.
Heliö K et al.
Frontiers in Cardiovascular Medicine, 2023
37795486 (PubMed )
Supplement: Table1.xlsx › Sheet1
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_MOESM3_ESM.xlsx › S1
LMOD2-related dilated cardiomyopathy presenting in late infancy.
Lay E et al.
American Journal of Medical Genetics. Part A, 2022
Early Death of 2 Siblings Related to Mutations in LMOD2, a Recently Discovered Cause of Neonatal Dilated Cardiomyopathy.
Greenway SC et al.
Cjc Open, 2021
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