Associated Papers
De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.
Anderson EN et al.
American Journal of Human Genetics, 2026
41468891 (PubMed )
Supplement: mmc2.xlsx › S7_KDM_genes_literature
Genotype-phenotype correlation study of structural abnormalities in a fetal brain caused by a novel KDM4B variant.
Zhao X et al.
Molecular Biology Reports, 2024
Human phenotype caused by biallelic KDM4B frameshift variant.
Takada S et al.
Clinical Genetics, 2024
Novel diagnostic DNA methylation episignatures expand and refine the epigenetic landscapes of Mendelian disorders.
Levy MA et al.
Hgg Advances, 2022
35047860 (PubMed )
Supplement: mmc2.xlsx › Table_S1_samples
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