Monozygotic twins with shared de novo GATA2 mutation but dissimilar phenotypes due to differential promoter methylation-Reference-Cited by-同舟云学术

Monozygotic twins with shared de novo GATA2 mutation but dissimilar phenotypes due to differential promoter methylation

Published:2019-02-04 Issue:4 Volume:60 Page:1053-1061
ISSN:1042-8194
Container-title:Leukemia & Lymphoma
language:en
Short-container-title:Leukemia & Lymphoma

Author:

Kim Namhee¹^ORCID,Choi Seongmin²,Kim Sung-Min³,Lee Amos Chungwon⁴,Im Kyongok³,Park Hee Sue¹,Kim Jung-Ah¹^ORCID,Kim Kwangsoo²,Kim Inho⁵,Chang Yoon Hwan⁶,Lee Dong Soon¹³

Affiliation:

1. Department of Laboratory Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea;

2. Division of Clinical Bioinformatics Biomedical Research Institute, Seoul National University Hospital, Seoul, Republic of Korea;

3. Cancer Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea;

4. Interdisciplinary program of Bioengineering, Seoul National University, Seoul, Republic of Korea;

5. Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea;

6. Department of Laboratory Medicine, Korea Cancer Center Hospital, Seoul, Republic of Korea

Funder

National Research Foundation of Korea

Ministry of Science, ICT and Future Planning

Korea Health Industry Development Institute

Ministry of Health & Welfare, Republic of Korea

Publisher

Informa UK Limited

Subject

Cancer Research,Oncology,Hematology

Link

https://www.tandfonline.com/doi/pdf/10.1080/10428194.2018.1516039

Reference39 articles.

1. The Origin and Evolution of Mutations in Acute Myeloid Leukemia

2. A targeted next-generation sequencing in the molecular risk stratification of adult acute myeloid leukemia: implications for clinical practice

3. Genomic and Epigenomic Landscapes of Adult De Novo Acute Myeloid Leukemia

4. Myeloid Neoplasms with Germline Predisposition

5. Proposal for the clinical detection and management of patients and their family members with familial myelodysplastic syndrome/acute leukemia predisposition syndromes

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