The burden of TTN variants in the genomic era: Analysis of 18,462 individuals from the Solve-RD consortium and general recommendations
Maria Francesca Di Feo(Folkhälsans Forskningscentrum), Mridul Johari(University of Helsinki), Mariëlle van Gijn, Leslie Matalonga Borrel(Centro Nacional de Análisis Genómico), Peter Hackman(Folkhälsans Forskningscentrum), Ana Töpf(Newcastle upon Tyne Hospitals NHS Foundation Trust), Richarda M. de Voer(Radboud University Nijmegen), Gisèle Bonne(Sorbonne Université), Lisenka E.L.M. Vissers(Radboud University Nijmegen), Gaëtan Lesca(Hospices Civils de Lyon), Simona Balestrini(Meyer Children's Hospital), Sergi Beltrán(Universitat de Barcelona), Mireille Cossée(Centre National de la Recherche Scientifique), Aurélien Perrin(Centre National de la Recherche Scientifique), Marco Savarese(Folkhälsans Forskningscentrum), Han Brunner(Radboud University Nijmegen), Holm Graessner(University Children's Hospital Tübingen), Holger Lerche(Hertie Institute for Clinical Brain Research), Kornelia Ellwanger(University of Tübingen), German Demidov(University of Tübingen), Anna Sarkozy(Great Ormond Street Hospital), B. Udd(Pirkanmaa Hospital District), Steven Laurie(Centro Nacional de Análisis Genómico), Job A.J. Verdonschot(Maastricht University Medical Centre), Swethaa Natraj Gayathri(Folkhälsans Forskningscentrum)
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