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Cracking rare disorders: a new minimally invasive RNA-seq protocol

Title:	Cracking rare disorders: a new minimally invasive RNA-seq protocol
Authors:	De Cock, Laurenz^{Aff1, Aff2, Aff3, Aff4}; D’haenens, Erika^Aff2; Vantomme, Lies^{Aff1, Aff2}; Backers, Lynn^{Aff1, Aff2, Aff3}; Beyens, Aude^{Aff1, Aff2}; Claes, Kathleen BM^{Aff1, Aff2, Aff3}; De Clercq, Griet^{Aff1, Aff2}; de Putter, Robin^Aff2; Kumps, Candy^Aff2; Schuermans, Nika^Aff2; Sourbron, Jo^Aff2; Syryn, Hannes^{Aff1, Aff2}; Tavernier, Simon^Aff2; Vanbelleghem, Eva^{Aff1, Aff2}; Vanakker, Olivier^{Aff1, Aff2}; Vandekerckhove, Bart^{Aff3, Aff4}; Van Damme, Tim^Aff2; Callewaert, Bert^{Aff1, Aff2}; Dheedene, Annelies^{Aff1, Aff2}; Vergult, Sarah^{Aff1, Aff2, IDs41525025005027_cor1}; Menten, Björn^{Aff1, Aff2, Aff3, IDs41525025005027_cor2}
Source:	npj Genomic Medicine. 10(1)
Database:	Springer Nature Journals