A randomized controlled trial of intranasal oxytocin in Phelan-McDermid syndrome
Abstract Background Phelan-McDermid syndrome (PMS) is a rare neurodevelopmental disorder caused by haploinsufficiency of the SHANK3 gene and characterized by global developmental delays, deficits in speech and motor function, and autism spectrum disorder (ASD). Monogenic causes of ASD such as PMS ar...
Main Authors: | , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2021-09-01
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Series: | Molecular Autism |
Subjects: | |
Online Access: | https://doi.org/10.1186/s13229-021-00459-1 |