Hematology
Volume 29, 2024 - Issue 1
Case Report
Identification of a novel splice variant in SEC23B gene in a patient with concomitant presence of congenital dyserythropoietic anemia II and Gilbert’s syndrome
Woori Janga Department of Laboratory Medicine, College of Medicine, Inha University, Incheon, Korea;c Northwest Gyeonggi Regional Center for Rare Disease, Incheon, Korea
https://orcid.org/0000-0001-8376-0133View further author information
https://orcid.org/0000-0001-8376-0133View further author information, Dong Jun Hab Department of Pediatrics, College of Medicine, Inha University, Incheon, Koreahttps://orcid.org/0000-0002-4331-6801View further author information
https://orcid.org/0000-0002-4331-6801View further author information, Chung Hyun Nahma Department of Laboratory Medicine, College of Medicine, Inha University, Incheon, Koreahttps://orcid.org/0000-0002-9721-0578View further author information
https://orcid.org/0000-0002-9721-0578View further author information, Jisun Parkb Department of Pediatrics, College of Medicine, Inha University, Incheon, Korea;c Northwest Gyeonggi Regional Center for Rare Disease, Incheon, Koreahttps://orcid.org/0000-0003-3793-6577View further author information
https://orcid.org/0000-0003-3793-6577View further author information, Su Jin Kimb Department of Pediatrics, College of Medicine, Inha University, Incheon, Korea;c Northwest Gyeonggi Regional Center for Rare Disease, Incheon, Koreahttps://orcid.org/0000-0003-0893-0512View further author information
https://orcid.org/0000-0003-0893-0512View further author information, Ji-Eun Leeb Department of Pediatrics, College of Medicine, Inha University, Incheon, Korea;c Northwest Gyeonggi Regional Center for Rare Disease, Incheon, KoreaCorrespondence[email protected]
https://orcid.org/0000-0002-7386-0015View further author information
https://orcid.org/0000-0002-7386-0015View further author information & Yeonsook Moona Department of Laboratory Medicine, College of Medicine, Inha University, Incheon, Korea;c Northwest Gyeonggi Regional Center for Rare Disease, Incheon, KoreaCorrespondence[email protected]
https://orcid.org/0000-0002-0135-6477View further author information
https://orcid.org/0000-0002-0135-6477View further author information show all