논문
쓰리빌리언의 연구 논문을 확인해보세요.
- Paper Title
- A homozygous in-frame duplication within the LRRCT consensus sequence of CFAP410 causes cone-rod dystrophy, macular staphyloma and short stature
- Journal Name, Publication year
- Ophthalmic genetics, 2021
- 링크
- https://www.tandfonline.com/doi/full/10.1080/13816810.2021.2010773
- Paper Title
- Hypomagnesemia and seizures in a patient with an SOS1 mutation
- Journal Name, Publication year
- Seizure, 2021
- 링크
- https://www.seizure-journal.com/article/S1059-1311(21)00317-4/fulltext
- Paper Title
- Compound heterozygote between point mutation and chromosomal microdeletion involving OTUD6B coinciding with ZMIZ1 variant in syndromic intellectual disability
- Journal Name, Publication year
- Genes, 2021
- 링크
- https://www.mdpi.com/2073-4425/12/10/1583
- Paper Title
- Phenotypic and Molecular Spectrum of Patients With Switch/sucrose Nonfermenting Complex-related Intellectual Disabilities in Korea
- Journal Name, Publication year
- BMC medical genomics, 2021
- 링크
- https://bmcmedgenomics.biomedcentral.com/articles/10.1186/s12920-021-01104-9
- Paper Title
- Clinical and genetic spectra in patients with dystrophinopathy in Korea: A single-center study
- Journal Name, Publication year
- Plos One, 2021
- 링크
- https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0255011
