Henrik Jensen

Protein expression studies of desmoplakin mutations in cardiomyopathy patients reveal different molecular disease mechanisms

P. Bross, J. Mogensen, U. Jensen, 2013, Clinical genetics.

The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark.

H. Jensen, Henrik Jensen, 2002, Danish medical bulletin.

Mutated Desmoglein‐2 Proteins are Incorporated into Desmosomes and Exhibit Dominant‐Negative Effects in Arrhythmogenic Right Ventricular Cardiomyopathy

P. Bross, J. Mogensen, U. Jensen, 2013, Human mutation.

Sudden Cardiac Death in Young Adults: Environmental Risk Factors and Genetic Aspects of Premature Atherosclerosis *,†

I. B. Kristensen, J. Banner, P. Nissen, 2012, Journal of forensic sciences.

Mutated Desmoglein‐2 Proteins are Incorporated into Desmosomes and Exhibit Dominant‐Negative Effects in Arrhythmogenic Right Ventricular Cardiomyopathy

P. Bross, J. Mogensen, U. Jensen, 2013, Human mutation.