British Journal of Haematology 2020-Apr
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.
Endast registrerade användare kan översätta artiklar
Logga in Bli medlem
Länken sparas på Urklipp