FAM53B truncation caused by t(10;19)(q26;q13) chromosome translocation in acute lymphoblastic leukemia

RNA-sequencing of the patient's bone marrow detected fusion transcripts in which the coding sequence of the FAM53B gene (from 10q26) was fused to a genomic sequence (from 19q13) that mapped upstream of the SLC7A10 locus. Reverse transcription-polymerase chain reaction together with Sanger seque...

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Detalles Bibliográficos
Autores principales: Panagopoulos, Ioannis, Gorunova, Ludmila, Torkildsen, Synne, Tierens, Anne, Heim, Sverre, Micci, Francesca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5403202/
https://www.ncbi.nlm.nih.gov/pubmed/28454383
http://dx.doi.org/10.3892/ol.2017.5705

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5403202/
https://www.ncbi.nlm.nih.gov/pubmed/28454383
http://dx.doi.org/10.3892/ol.2017.5705

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