Associated Papers
Frequency enrichment of coding variants in a French-Canadian founder population and its implication for inflammatory bowel diseases.
Bhérer C et al.
Medrxiv : the Preprint Server for Health Sciences, 2025
40791678 (PubMed )
Supplement: media-2.xlsx › Table_S12_ClinVar_PLP_variants
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
Further delineation of METTL23-associated intellectual disability.
Almannai M et al.
American Journal of Medical Genetics. Part A, 2020
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