This is the author accepted manuscript. The final version is available from Nature via the DOI in this record.The genomes of individuals with severe, undiagnosed developmental disorders are enriched in damaging de novo mutations (DNMs) in developmentally important genes. Here we have sequenced the exomes of 4,293 families containing individuals with developmental disorders, and meta-analysed these data with data from another 3,287 individuals with similar disorders. We show that the most important factors influencing the diagnostic yield of DNMs are the sex of the affected individual, the relatedness of their parents, whether close relatives are affected and the parental ages. We identified 94 genes enriched in damaging DNMs, including 14 t...
The genomes of individuals with severe, undiagnosed developmental disorders are enriched in damaging...
The genomes of individuals with severe, undiagnosed developmental disorders are enriched in damaging...
De novo mutations in protein-coding genes are a well-established cause of developmental disorders1. ...
The genomes of individuals with severe, undiagnosed developmental disorders are enriched in damaging...
The genomes of individuals with severe, undiagnosed developmental disorders are enriched in damaging...
De novo mutations in protein-coding genes are a well-established cause of developmental disorders1. ...
The genomes of individuals with severe, undiagnosed developmental disorders are enriched in damaging...
The genomes of individuals with severe, undiagnosed developmental disorders are enriched in damaging...
De novo mutations in protein-coding genes are a well-established cause of developmental disorders1. ...