|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||defects in the suppressive response of central synapses when activated twice in rapid succession; indicative of defects in short-term plasticity due to lack of inhibition of neurotransmitter release at the second stimulus (Mammalian Phenotype Ontology, MP_0004807)|
|Downloads & Tools|
7 gene mutations causing the abnormal paired-pulse inhibition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.