Associated Papers
Integrated Analysis of WES and scRNA-Seq Data Reveals the Genetic Basis of Immune Dysregulation in Unexplained Recurrent Pregnancy Loss.
Lin ZJ et al.
Journal of Clinical Laboratory Analysis, 2025
40066928 (PubMed )
Supplement: JCLA-39-e70011-s001.xlsx › sTable-4._Mutation_infomation
Expanding the clinical phenotype of FADD deficiency with a novel mutation and its role in Fas-mediated apoptotic pathway.
Setia P et al.
British Journal of Haematology, 2023
37199216 (PubMed )
Supplement: supplement_1.docx
Bioinformatic prediction of putative conveyers of O-GlcNAc transferase intellectual disability.
Mitchell CW et al.
The Journal of Biological Chemistry, 2022
35863433 (PubMed )
Supplement: mmc4.xlsx › -4_position
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