Biallelic Variants in POPDC2 Cause a Novel Autosomal Recessive Syndrome Presenting with Cardiac Conduction Defects and Variable 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 Santome , David 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 , Kári Stefánsson , Lincoln Nadauld , Kirk U Knowlton , Sisse Rye Ostrowski , Erik Sørensen , Ole Birger Vesterager Pedersen , Jonas Ghouse , Søren 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 American journal of human genetics（2025）
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