Cracking rare disorders: a new minimally invasive RNA-seq protocol by Laurenz De Cock, Erika D’haenens, Lies Vantomme, Lynn Backers, Aude Beyens, Kathleen BM Claes, Griet De Clercq, Robin de Putter, Candy Kumps, Nika Schuermans, Jo Sourbron, Hannes Syryn, Simon Tavernier, Eva Vanbelleghem, Olivier Vanakker, Bart Vandekerckhove, Tim Van Damme, Bert Callewaert, Annelies Dheedene, Sarah Vergult, Björn Menten

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