Unraveling the Genetic Landscape of Langerhans Cell Histiocytosis in Korean Patients: Comprehensive Insights from Mutational Profiles and Clinical Correlations
This study identified mutually exclusive MAPK pathway mutations in every LCH patient through comprehensive genetic analysis, highlighting the importance of inclusive testing in understanding the disease's genetics.
Authors
- Kyung‐Nam Koh (ORCID: https://orcid.org/0000-0002-6376-672X)
- Sung‐Min Chun (ORCID: https://orcid.org/0000-0002-3357-1382)
- Su Hyun Yoon (ORCID: https://orcid.org/0000-0002-5817-0278)
- Hyery Kim (ORCID: https://orcid.org/0000-0003-2852-6832)
- Sung Han Kang (ORCID: https://orcid.org/0000-0002-1651-4415)
- Young Kwon Koh
- Ho Joon Im (ORCID: https://orcid.org/0000-0001-8799-4068)
- Ha Ra Jun
- Ji Young Kim (ORCID: https://orcid.org/0000-0003-1466-2112)
- Ji‐Young Lee (ORCID: https://orcid.org/0000-0002-3301-6434)
Institutions
- Ulsan College (KR)
- Chosun University (KR)
- Asan Medical Center (KR)
- University of Ulsan (KR)
Publication Details
- Journal
- Cancer Research and Treatment
- Published
- 2024-12-24
- DOI
- https://doi.org/10.4143/crt.2024.782
- Citations
- 2
- Primary Topic
- Histiocytic Disorders and Treatments
- Type
- article
- Field-Weighted Citation Impact
- 0.65
Funders
- Korea Disease Control and Prevention Agency
- Asan Institute for Life Sciences, Asan Medical Center