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in Clin Genet

Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3

J. Kühnisch et al.
in J Am Heart Assoc

RIKADA study reveals risk factors in pediatric primary cardiomyopathy

N. Al-Wakeel-Marquard et al.
in Cell

The translational landscape of the human heart

S. van Heesch et al.
in J Am Coll Cardiol

Left ventricular noncompaction: phenotype in an integrated model of cardiomyopathy?

E. Oechslin et al.
in Int J Cardiol

Left ventricular non-compaction: prevalence in congenital heart disease

B.E. Stähli et al.
in Am J Med Genet C Semin Med Genet

Ebstein anomaly associated with left ventricular noncompaction: an autosomal dominant condition that can be caused by mutations in MYH7

A.M. Vermeer et al.
in Am J Hum Genet

Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy

A.K. Arndt et al.
in Neth Heart J

Ebstein's anomaly may be caused by mutations in the sarcomere protein gene MYH7

K. van Engelen et al.