Associated Papers
Rare predicted deleterious FEZF2 variants are associated with a neurodevelopmental phenotype.
Garber A et al.
American Journal of Medical Genetics. Part A, 2024
Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes.
Feliciano P et al.
Npj Genomic Medicine, 2019
31452935 (PubMed )
Supplement: 41525_2019_93_MOESM12_ESM.xlsx › de_novo_SNV_indel
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