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

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Bibliographic Details
Published in:British journal of haematology 2020-05, Vol.189 (4), p.e182-e184
Main Authors: López‐Andrade, Bernardo, Bento, Leyre, Diez Campelo, Maria, López Cadenas, Félix, González Martín, Teresa, Lo Riso, Laura, Novo, Andres, Martinez‐Serra, Jorge, Ballester, Carmen, Sampol, Antonia, Duran, Maria Antonia
Format: Article
Language:English
Subjects:
Adult
Case reports
Gene polymorphism
Hematology
Hematopoietic Stem Cell Transplantation - methods
Hematopoietic stem cells
High-Throughput Nucleotide Sequencing - methods
Humans
Male
Myelodysplastic syndrome
Myelodysplastic Syndromes - genetics
Myelodysplastic Syndromes - therapy
Polymorphism, Genetic
Protein-tyrosine kinase
Stem cell transplantation
Transplantation Conditioning - methods
Transplantation, Homologous
TYK2 Kinase - genetics
Tyk2 protein
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ISSN:0007-1048
1365-2141
DOI:10.1111/bjh.16590