Cracking rare disorders: a new minimally invasive RNA-seq protocol
破解罕见疾病：一种新的微创RNA测序方案
期刊:npj Genomic Medicine
影响因子:4.7
doi:10.1038/s41525-025-00502-7
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
