Complex movement disorders associated with DEAF1 gene mutation-Reference-Cited by-同舟云学术

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Complex movement disorders associated with DEAF1 gene mutation

Published:2024-09 Issue: Volume:126 Page:107055
ISSN:1353-8020
Container-title:Parkinsonism & Related Disorders
language:en
Short-container-title:Parkinsonism & Related Disorders

Author:

Rebelo Procaci Victor^ORCID,Goulart Leonardo Ierardi,Ferraz Henrique Ballalai,Povoas Barsottini Orlando Graziani,Pedroso José Luiz

Publisher

Elsevier BV

Reference5 articles.

1. De novo and biallelic DEAF1 variants cause a phenotypic spectrum;Nabais;Genet. Med.,2019

2. Recessive DEAF1 mutation associates with autism, intellectual disability, basal ganglia dysfunction and epilepsy;Rajab;J. Med. Genet.,2015

3. Varieties of repetitive behavior in autism: comparisons to mental retardation;Bodfish;J. Autism Dev. Disord.,2000

4. Autism and Asperger's disorder: are they movement disorders involving the cerebellum and/or basal ganglia?;Nayate;Brain Res. Bull.,2005

5. Diagnostic approach to paediatric movement disorders: a clinical practice guide;Brandsma;Dev. Med. Child Neurol.,2021

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