关键词: QRICH1 Ververi-Brady syndrome autism spectrum disorder language development disorders
Mesh : Adolescent Child Child, Preschool Codon, Nonsense / genetics DNA-Binding Proteins / genetics Developmental Disabilities / diagnostic imaging genetics pathology Exome / genetics Female Frameshift Mutation / genetics Genetic Predisposition to Disease Genotype Humans Intellectual Disability / diagnostic imaging genetics pathology Loss of Function Mutation / genetics Male Mutation, Missense / genetics Phenotype Transcription Factors / genetics
来 源:
DOI:10.1111/cge.13853
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