The arrhythmogenic cardiomyopathy phenotype associated with PKP2 c.1211dup variant

Thomas A. Bos, Sebastiaan R.D. Piers, Marja W. Wessels, Arjan C. Houweling, Regina Bökenkamp, Marianne Bootsma, Laurens P. Bosman, Reinder Evertz, Debby M.E.I. Hellebrekers, Yvonne M. Hoedemaekers, Jeroen Knijnenburg, Ronald Lekanne Deprez, Anneke M. van Mil, Anneline S.J.M. te Riele, Marjon A. van Slegtenhorst, Arthur A.M. Wilde, Sing Chien Yap, Dennis Dooijes, Tamara T. Koopmann, J. Peter van TintelenDaniela Q.C.M. Barge-Schaapveld*, European Reference Network for rare, low prevalence and complex diseases of the heart: ERN GUARD-Heart

*Corresponding author for this work

Research output: Contribution to journal › Article › Academic › peer-review

Fingerprint

Dive into the research topics of 'The arrhythmogenic cardiomyopathy phenotype associated with PKP2 c.1211dup variant'. Together they form a unique fingerprint.

Keyphrases

Biochemistry, Genetics and Molecular Biology

INIS