A Case of NEDMAGA: Neurodevelopmental Disorder with Movement Abnormalities, Abnormal Gait, and Autistic Features
Author:
Affiliation:
1. Department of Neurology Santa Marcelina Hospital São Paulo Brazil
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Reference8 articles.
1. A Recurrent De Novo Nonsense Variant in ZSWIM6 Results in Severe Intellectual Disability without Frontonasal or Limb Malformations
2. Loss of the neurodevelopmental gene Zswim6 alters striatal morphology and motor regulation
3. Exome Sequencing Identifies a Recurrent De Novo ZSWIM6 Mutation Associated with Acromelic Frontonasal Dysostosis
4. Acromelic frontonasal dysostosis andZSWIM6mutation: phenotypic spectrum and mosaicism
5. Genetic testing in individuals with cerebral palsy
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