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

  1. López-Andrade, B.
  2. Bento, L.
  3. Diez Campelo, M.
  4. López Cadenas, F.
  5. González Martín, T.
  6. Lo Riso, L.
  7. Novo, A.
  8. Martinez-Serra, J.
  9. Ballester, C.
  10. Sampol, A.
  11. Duran, M.A.
Revista:
British Journal of Haematology

ISSN: 1365-2141,  0007-1048

Ano de publicación: 2020

Volume: 189

Número: 4

Páxinas: e182-e184

Tipo: Carta

DOI: 10.1111/BJH.16590 GOOGLE SCHOLAR lock_openAcceso aberto editor
Fonte de datos: Scopus