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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
Author(s) -
LópezAndrade Bernardo,
Bento Leyre,
Diez Campelo Maria,
López Cadenas Félix,
González Martín Teresa,
Lo Riso Laura,
Novo Andres,
MartinezSerra Jorge,
Ballester Carmen,
Sampol Antonia,
Duran Maria Antonia
Publication year - 2020
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1111/bjh.16590
Subject(s) - transplantation , medicine , myelodysplastic syndromes , minimal residual disease , hematopoietic stem cell transplantation , oncology , stem cell , bioinformatics , leukemia , bone marrow , biology , genetics
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