Discriminating a common somatic ASXL1 mutation (c.1934dup; p.G646Wfs12) from artifact in myeloid malignancies using NGS

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Veröffentlicht in:	Leukemia 2018-08, Vol.32 (8), p.1874-1878
Hauptverfasser:	Alberti, Michael O., Srivatsan, Sridhar Nonavinkere, Shao, Jin, McNulty, Samantha N., Chang, Gue Su, Miller, Christopher A., Dunlap, Jennifer B., Yang, Fei, Press, Richard D., Gao, Qingsong, Ding, Li, Heusel, Jonathan W., Duncavage, Eric J., Walter, Matthew J.
Format:	Artikel
Sprache:	eng
Schlagworte:	45 45/22 45/23 631/67/69 692/699/67/1990/1673 692/699/67/69 692/700/139/1512 Acute myelocytic leukemia Biomarkers, Tumor - genetics Brief Communication Cancer Cancer Research Care and treatment Critical Care Medicine Diagnosis, Differential Gene Duplication Gene mutation Genetic aspects Hematologic Neoplasms - diagnosis Hematologic Neoplasms - genetics Hematology High-Throughput Nucleotide Sequencing - methods High-Throughput Nucleotide Sequencing - standards Humans Intensive Internal Medicine Medical schools Medicine Medicine & Public Health Molecular Diagnostic Techniques Mutation Myeloproliferative Disorders - diagnosis Myeloproliferative Disorders - genetics Oncology Polymerase chain reaction Prognosis Repressor Proteins - genetics Universities and colleges
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