The implication of 'unknown significance' variants in next-generation sequencing in diagnosis and donor selection for allogenic haematopoietic stem cell transplantation. Report of a case of myelodysplastic syndrome with a polymorphism in the tyrosine kinase 2 (TYK2) gene.
Bernardo López AndradeLeyre BentoMaria Diez CampeloFélix López CadenasTeresa González MartínLaura Lo RisoAndres NovoJorge Martinez-SerraCarmen BallesterAntonia SampolMaria Antonia DuranPublished in: British journal of haematology (2020)