Cracking rare disorders: a new minimally invasive RNA-seq protocol.
攻克罕见疾病:一种新的微创 RNA 测序方案
期刊:npj Genomic Medicine
影响因子:4.800
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