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by Lee, SE and Choi, JY and Kim, SE and Kim, SC
EUROPEAN JOURNAL OF DERMATOLOGY, ISSN 1167-1122, 01/2018, Volume 28, Issue 1, pp. 123 - 125
Journal Article
Pathology and Oncology Research, ISSN 1219-4956, 06/2018, pp. 1 - 2
Journal Article
Pathology and Oncology Research, ISSN 1219-4956, 03/2018, pp. 1 - 2
Journal Article
Cancer Research, ISSN 0008-5472, 09/2015, Volume 75, Issue 17, pp. 3446 - 3455
Journal Article
Gene, ISSN 0378-1119, 10/2019, p. 144226
Journal Article
Journal Article
Journal Article
European Journal of Haematology, ISSN 0902-4441, 08/2018, Volume 101, Issue 2, pp. 216 - 219
Somatic CALR mutations have been identified in the majority of JAK2 mutation‐negative essential thrombocythaemia (ET) and primary myelofibrosis. Almost all... 
CALR mutation | 2‐base pair frameshift | double mutations | myeloproliferative neoplasm | 2-base pair frameshift | HEMATOLOGY | CALRETICULIN | Development and progression | Genetic aspects | Tumors | Headache | Myelofibrosis | Janus kinase 2 | Amino acid sequence | Frameshift mutation | Tumorigenesis | Mutation
Journal Article
Meta Gene, ISSN 2214-5400, 12/2017, Volume 14, pp. 30 - 32
Hereditary Hemochromatosis is a genetic disorder characterized by disrupted iron metabolism related to gene defects altering the expression of regulatory... 
Hemochromatosis | Novel | Frameshift | Mutation
Journal Article
Pathology - Research and Practice, ISSN 0344-0338, 08/2019, Volume 215, Issue 8, p. 152453
The truncating mutations of RNF43 frequently occur in CRC, we aimed to clarify the relationship between RNF43 frameshift mutations and MS status, BRAF V600E... 
Frameshift mutation | RNF43 | Microsatellite status | Colorectal cancer
Journal Article
Journal Article