Single point mutation on the gene encoding dysbindin results in recognition deficits. [electronic resource]
Producer: 20181030Description: e12449 p. digitalISSN:- 1601-183X
- Animals
- Behavior, Animal
- Cognition Disorders -- genetics
- Disease Models, Animal
- Dysbindin -- genetics
- Female
- Haplotypes
- Hippocampus -- metabolism
- Homozygote
- Male
- Memory, Short-Term
- Mice
- Mice, Inbred C57BL
- Mice, Knockout
- Point Mutation
- Polymorphism, Single Nucleotide -- genetics
- Prefrontal Cortex -- metabolism
- Recognition, Psychology -- physiology
- Schizophrenia -- genetics
- Synaptosomal-Associated Protein 25 -- genetics
No physical items for this record
Publication Type: Journal Article; Research Support, N.I.H., Extramural
There are no comments on this title.
Log in to your account to post a comment.