Rare genetic variants in CX3CR1 and their contribution to the increased risk of schizophrenia and autism spectrum disorders. [electronic resource]
Producer: 20180503Description: e1184 p. digitalISSN:- 2158-3188
- Adolescent
- Adult
- Aged
- Autism Spectrum Disorder -- genetics
- CX3C Chemokine Receptor 1 -- genetics
- Child
- Computer Simulation
- Exons
- Female
- Genetic Association Studies
- Genetic Predisposition to Disease
- Genotype
- High-Throughput Nucleotide Sequencing
- Humans
- Male
- Middle Aged
- Mutation
- Polymorphism, Single Nucleotide
- Schizophrenia -- genetics
- Young Adult
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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