RNA-sequencing unveils FLT4 splice site variants in variable congenital heart disease von Verlee, Maxim, D'haenens, Erika, De Cock, Laurenz, Muiño Mosquera, Laura, De Groote, Katya, Vandekerckhove, Kristof, Panzer, Joseph, Roets, Ellen, Menten, Björn, Symoens, Sofie, Coucke, Paul, Vandamme, Tim, Vergult, Sarah, Callewaert, Bert

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Loss-of-Function Variants in EFEMP1 Cause a Recognizable Connective Tissue Disorder Characterized by Cutis Laxa and Multiple Herniations von Verlee, Maxim, Beyens, Aude, Gezdirici, Alper, Gulec, Elif Yilmaz, Pottie, Lore, De Feyter, Silke, Vanhooydonck, Michiel, Tapaneeyaphan, Piyanoot, Symoens, Sofie, Callewaert, Bert

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Loss-of-function variants in EFEMP1 cause a recognizable connective tissue disorder characterized by cutis laxa and multiple herniations von Verlee, Maxim, Beyens, Aude, Gezdirici, Alper, Gulec, Elif, Pottie, Lore, De Feyter, Silke, Vanhooydonck, Michiel, Tapaneeyaphan, Piyanoot, Symoens, Sofie, Callewaert, Bert

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Loss-of-Function Variants in EFEMP1 Cause a Recognizable Connective Tissue Disorder Characterized by Cutis Laxa and Multiple Herniations von Verlee, Maxim, Beyens, Aude, Gezdirici, Alper, Gulec, Elif Yilmaz, Pottie, Lore, De Feyter, Silke, Vanhooydonck, Michiel, Tapaneeyaphan, Piyanoot, Symoens, Sofie, Callewaert, Bert

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