| Dataset | MPO Gene-Phenotype Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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) |
| External Link | http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004807 |
| Similar Terms | |
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7 gene mutations causing the abnormal paired-pulse inhibition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
