טוען...
SETD2 and histone H3 lysine 36 methylation deficiency in advanced systemic mastocytosis
The molecular basis of advanced systemic mastocytosis (SM) is not fully understood and despite novel therapies the prognosis remains dismal. Exome sequencing of an index-patient with mast cell leukemia (MCL) uncovered biallelic loss-of-function mutations in the SETD2 histone methyltransferase gene....
שמור ב:
| הוצא לאור ב: | Leukemia |
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Nature Publishing Group
2018
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5770597/ https://ncbi.nlm.nih.gov/pubmed/28663576 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/leu.2017.183 |
| תגים: |
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