Ebstein anomaly associated with left ventricular noncompaction: an autosomal dominant condition that can be caused by mutations in MYH7.
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Genetic testing in congenital heart disease: A clinical approachLoss of Function Mutations in NNT Are Associated With Left Ventricular NoncompactionGenetics and disease of ventricular muscle.Heart failure in congenital heart disease: the role of genes and hemodynamics.Non-compaction cardiomyopathy: prevalence, prognosis, pathoetiology, genetics, and risk of cardioembolism.Ebstein anomaly: assessment, management, and timing of intervention.
P2860
Ebstein anomaly associated with left ventricular noncompaction: an autosomal dominant condition that can be caused by mutations in MYH7.
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Ebstein anomaly associated wit ...... e caused by mutations in MYH7.
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Ebstein anomaly associated wit ...... e caused by mutations in MYH7.
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Ebstein anomaly associated wit ...... e caused by mutations in MYH7.
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P2093
P2860
P356
P1476
Ebstein anomaly associated wit ...... be caused by mutations in MYH7
@en
P2093
Alexa M C Vermeer
Barbara J M Mulder
Bernard Keavney
Imke Christiaans
Klaartje van Engelen
Marieke J H Baars
Sabine Klaassen
Simone De Haij
P2860
P304
P356
10.1002/AJMG.C.31365
P577
2013-06-21T00:00:00Z