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
- López-Andrade, B.
- Bento, L.
- Diez Campelo, M.
- López Cadenas, F.
- González Martín, T.
- Lo Riso, L.
- Novo, A.
- Martinez-Serra, J.
- Ballester, C.
- Sampol, A.
- Duran, M.A.
ISSN: 1365-2141, 0007-1048
Ano de publicación: 2020
Volume: 189
Número: 4
Páxinas: e182-e184
Tipo: Carta