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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 J Am Coll Cardiol

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

E. Oechslin et al.
in Dtsch Med Wochenschr

Position paper of cardiovascular disease : genetic diagnostics in cardiovascular diseases [Positionspapier Kardiovaskulaere Erkrankungen: Gendiagnostik bei kardiovaskulaeren Erkrankungen ]

E. Schulze-Bahr et al.
in Circ Cardiovasc Genet

Malformations of the left ventricle: what comes first: form or function?

S. Klaassen
in Kardiologe

Gendiagnostik bei kardiovaskulären Erkrankungen: Positionspapier der Deutschen Gesellschaft für Kardiologie (DGK) und der Deutschen Gesellschaft für Pädiatrische Kardiologie (DGPK) [Molecular diagnostics of cardiovascular diseases: Expert consensus st

E. Schulze-Bahr 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.