Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy
Michele Nicastro, Alexa M. C. Vermeer, Pieter G. Postema, Rafik Tadros, Forrest Z. Bowling, Hildur M. Aegisdottir, Vinicius Tragante, Lukas Mach, Alex V. Postma, Elisabeth M. Lodder, Karel van Duijvenboden, Rob Zwart, Leander Beekman, Lingshuang Wu, Sean J. Jurgens, Paul A. van der Zwaag, Mariëlle Alders, Mona Allouba, Yasmine Aguib, J. Luis SantomeDavid de Una, Lorenzo Monserrat, Antonio M. A. Miranda, Kazumasa Kanemaru, James Cranley, Ingeborg E. van Zeggeren, Eleonora M. A. Aronica, Michela Ripolone, Simona Zanotti, Gardar Sveinbjornsson, Erna V. Ivarsdottir, Hilma Hólm, Daníel F. Guðbjartsson, Ástrós Th. Skúladóttir, K. ri Stefánsson, Lincoln Nadauld, Kirk U. Knowlton, Sisse Rye Ostrowski, Erik Sørensen, Ole Birger Vesterager Pedersen, Jonas Ghouse, S. ren A. Rand, Henning Bundgaard, Henrik Ullum, Christian Erikstrup, Bitten Aagaard, Mie Topholm Bruun, Mette Christiansen, Henrik K. Jensen, Deanna Alexis Carere, Christopher T. Cummings, Kristen Fishler, Pernille Mathiesen tørring, Klaus Brusgaard, Trine Maxel Juul, Lotte Saaby, Bo Gregers Winkel, Jens Mogensen, Francesco Fortunato, Giacomo Pietro Comi, Dario Ronchi, J. Peter van Tintelen, Michela Noseda, Michael V. Airola, Imke Christiaans, Arthur A. M. Wilde, Ronald Wilders, Sally-Ann Clur, Arie O. Verkerk, Connie R. Bezzina, Najim Lahrouchi*
Research output: Contribution to journal › Article › Academic › peer-review
Fingerprint
Dive into the research topics of 'Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy'. Together they form a unique fingerprint.