Associated Papers
Dilated cardiomyopathy in patients with PRDM16 haploinsufficiency.
Billon C et al.
Journal of Molecular Medicine (berlin, Germany), 2025
The Trouble with Trabeculation: How Genetics Can Help to Unravel a Complex and Controversial Phenotype.
Walsh R
Journal of Cardiovascular Translational Research, 2023
Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies.
Mazzarotto F et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2021
33500567 (PubMed )
Supplement: 41436_2020_1049_MOESM2_ESM.xlsx › Table_S2
Cardiomyopathy due to PRDM16 mutation: First description of a fetal presentation, with possible modifier genes.
Delplancq G et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics, 2020
Systematic Review of Genotype-Phenotype Correlations in Noncompaction Cardiomyopathy.
van Waning JI et al.
Journal of the American Heart Association, 2019
Select a paper to view details