Schizophrenia: Genome, Interrupted
نویسندگان
چکیده
Structural chromosomal variation is increasingly recognized as an important contributor to human diseases, particularly those of neurodevelopment, such as autism. A current paper makes a significant advance to schizophrenia genetics by establishing an association with rare copy number variants (CNV), which are over-represented in neurodevelopmental genes.
منابع مشابه
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عنوان ژورنال:
- Neuron
دوره 58 شماره
صفحات -
تاریخ انتشار 2008