Mutation in familial platelet disorder with predisposition to myeloid malignancies

ABSTRACT: Detection of causal variant for thrombocytopenia and second hit causing malignant disease onset by next-generation sequencing. The sample was taken at MDS diagnosis, the illness later developed into AML.

INSTRUMENT(S): NextSeq 500

ORGANISM(S): Homo sapiens

SUBMITTER: Lenka Radova 

PROVIDER: E-MTAB-6899 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress