The most commonly reported variant in ASXL1 (c.1934dupG;p.Gly646TrpfsX12) is not a somatic alteration Journal Article

   

Authors:	Abdel-Wahab, O.; Kilpivaara, O.; Patel, J.; Busque, L.; Levine, R. L.
Article Title:	The most commonly reported variant in ASXL1 (c.1934dupG;p.Gly646TrpfsX12) is not a somatic alteration
Keywords:	acute granulocytic leukemia; chronic myelomonocytic leukemia; gene sequence; frameshift mutation; missense mutation; mutation; stop codon; letter; allele; genetic variability; chronic myeloid leukemia; tumor suppressor gene; myelodysplastic syndrome; gene identification; nucleotide sequence; gene duplication; base pairing; dna sequence; gene insertion; repressor proteins; dna extraction; nonsense mutation; nucleotide repeat; downstream processing; open reading frame; guanine nucleotide; asxl1 gene; base mispairing
Journal Title:	Leukemia
Volume:	24
Issue:	9
ISSN:	0887-6924
Publisher:	Nature Publishing Group
Date Published:	2010-09-01
Start Page:	1656
End Page:	1664
Language:	English
DOI:	10.1038/leu.2010.144
PUBMED:	20596031
PROVIDER:	scopus
PMCID:	PMC4654627
DOI/URL:	http://www.scopus.com/inward/record.url?eid=2-s2.0-77956440933&partnerID=40&md5=d5d1f9e542fbb386263f1e8fc41617ee
Notes:	--- - "Cited By (since 1996): 3" - "Export Date: 20 April 2011" - "CODEN: LEUKE" - "Source: Scopus"

https://synapse.mskcc.org/synapse/works/has_related_data_chk/3554