关键词: Pitt-Hopkins-like syndrome 2 autism spectrum disorder compound heterozygosity developmental delay neurexin 1 schizophrenia
Mesh : Calcium-Binding Proteins / deficiency genetics Cell Adhesion Molecules, Neuronal / genetics Genetic Predisposition to Disease Humans Intellectual Disability / genetics pathology Mental Disorders / genetics pathology Mutation Nervous System Diseases / genetics pathology Neural Cell Adhesion Molecules / deficiency genetics Neurodevelopmental Disorders / genetics pathology Phenotype
来 源:
DOI:10.1111/cge.13537
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