Chong Kun Cheon
14PUBLICATIONS
54CO-AUTHORS

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Publications (14)
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|Mar 06, 2026
PRPS1 (p.V42L) Mutation in Arts Syndrome Induces Aberrant Neural Stem Cell Development and Neuronal Senescence-Like Phenotype: Rescue by Nicotinamide Mononucleotide Supplementation.Ji-Hee Kim, Su-Jung Park, Jeong-A Lee
|Dec 03, 2025
[Achievements and Expectations of the Rare Disease Diagnostic Support Program in the Republic of Korea].Ye Eun Lee, Jee Young Kim, Jun Kil Choi
|Jul 12, 2025
Multidisciplinary Care Model as a Center of Excellence for Fabry Disease: A Practical Guide to Diagnosis and Management by Clinical Specialty in South Korea.Soo Yong Lee, Il Young Kim, Sung-Ho Ahn
|Apr 14, 2025
Genome Sequencing of Rare Disease Patients Through the Korean Regional Rare Disease Diagnostic Support Program.Rin Khang, Hane Lee, Jihye Kim
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Frequent Collaborators
2 joint publications
Sukdong Yoo
1 joint publications
Young A Kim
1 joint publications
Seong Heon Kim
1 joint publications
Yoo Mi Kim
1 joint publications
Gilyazetdinov Kamil
1 joint publications
Ju Young Yoon
1 joint publications
Yun Hak Kim
1 joint publications
Rin Khang
1 joint publications
Hane Lee
1 joint publications
Jihye Kim