General Information:
Id: | 5,421 (click here to show other Interactions for entry) |
Diseases: |
Metabolic
Neurological |
Homo sapiens | |
article | |
Reference: | Saito M et al.(2014) MAOA/B deletion syndrome in male siblings with severe developmental delay and sudden loss of muscle tonus Brain Dev. 36: 64-69 [PMID: 23414621] |
Interaction Information:
Comment | Deletion of the monoamine oxidase (MAO)-A and MAO-B was detected in two male siblings and in their mother. The serotonin levels in their cerebrospinal fluid were extremely elevated. |
Formal Description Interaction-ID: 102619 |
phenotype decreased MAOB level increases_quantity of drug/chemical compound |