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5’UTR point substitutions and N-terminal truncating mutations of ANKRD26 in acute myeloid leukemia
Thrombocytopenia 2 (THC2) is an inherited disorder caused by monoallelic single nucleotide substitutions in the 5’UTR of the ANKRD26 gene. Patients have thrombocytopenia and increased risk of myeloid malignancies, in particular, acute myeloid leukemia (AML). Given the association of variants in the...
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| Pubblicato in: | J Hematol Oncol |
|---|---|
| Autori principali: | , , , , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2017
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5242010/ https://ncbi.nlm.nih.gov/pubmed/28100250 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13045-016-0382-y |
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