Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy
Titel:
Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy
Auteur:
Nicastro, Michele Vermeer, Alexa M.C. Postema, Pieter G. Tadros, Rafik Bowling, Forrest Z. Aegisdottir, Hildur M. Tragante, Vinicius Mach, Lukas Postma, Alex V. Lodder, Elisabeth M. van Duijvenboden, Karel Zwart, Rob Beekman, Leander Wu, Lingshuang Jurgens, Sean J. van der Zwaag, Paul A. Alders, Mariëlle Allouba, Mona Aguib, Yasmine Santome, J. Luis de Una, David Monserrat, Lorenzo Miranda, Antonio M.A. Kanemaru, Kazumasa Cranley, James van Zeggeren, Ingeborg E. Aronica, Eleonora M.A. Ripolone, Michela Zanotti, Simona Sveinbjornsson, Gardar Ivarsdottir, Erna V. Hólm, Hilma Guðbjartsson, Daníel F. Skúladóttir, Ástrós Th. Stefánsson, Kári Nadauld, Lincoln Knowlton, Kirk U. Ostrowski, Sisse Rye Sørensen, Erik Vesterager Pedersen, Ole Birger Ghouse, Jonas Rand, Søren A. Bundgaard, Henning Ullum, Henrik Erikstrup, Christian Aagaard, Bitten Bruun, Mie Topholm Christiansen, Mette Jensen, Henrik K. Carere, Deanna Alexis Cummings, Christopher T. Fishler, Kristen Tørring, Pernille Mathiesen Brusgaard, Klaus Juul, Trine Maxel Saaby, Lotte Winkel, Bo Gregers Mogensen, Jens Fortunato, Francesco Comi, Giacomo Pietro Ronchi, Dario van Tintelen, J. Peter Noseda, Michela Airola, Michael V. Christiaans, Imke Wilde, Arthur A.M. Wilders, Ronald Clur, Sally-Ann Verkerk, Arie O. Bezzina, Connie R. Lahrouchi, Najim