Associated Papers
Arab founder variants: Contributions to clinical genomics and precision medicine.
AlAbdi L et al.
Med (new York, N.y.), 2025
Identification of a novel METTL23 gene variant in a patient with an intellectual development disorder: a literature review and case report.
Zha J et al.
Frontiers in Pediatrics, 2024
Two Cases of Recessive Intellectual Disability Caused by NDST1 and METTL23 Variants.
Khan A et al.
Genes, 2020
Analysis of transcript-deleterious variants in Mendelian disorders: implications for RNA-based diagnostics.
Maddirevula S et al.
Genome Biology, 2020
32552793 (PubMed )
Supplement: 13059_2020_2053_MOESM3_ESM.xlsx › Table_S2
Further delineation of METTL23-associated intellectual disability.
Almannai M et al.
American Journal of Medical Genetics. Part A, 2020
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