Clinical, biochemical, and neuropsychiatric evaluation of a patient with a contiguous gene syndrome due to a microdeletion Xp11.3 including the Norrie disease locus and monoamine oxidase (MAOA andMAOB) genes
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference50 articles.
1. Serotonin in human lumbar cerebrospinal fluid: A reassessment
2. The natural history of amine oxidases
3. Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosome
4. Properties of monoamine oxidase (MAO) in human blood platelets, plasma, lymphocytes and granulocytes
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