Cognitive Assessment in GNAO1 Neurodevelopmental Disorder Using an Eye Tracking System
Cognitive Assessment in GNAO1 Neurodevelopmental Disorder Using an Eye Tracking System
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Publisher
Basel: MDPI AG
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Language
English
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Publisher
Basel: MDPI AG
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Scope and Contents
Contents
GNAO1 gene mutations are associated with a neurodevelopmental disorder characterized by developmental delay, epilepsy, and movement disorder. Eye tracking and eye movement analysis are an intriguing method to assess cognitive and language function and, to the best of our knowledge, it has never been tested in a standardized way in GNAO1. GNAO1 chil...
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Full title
Cognitive Assessment in GNAO1 Neurodevelopmental Disorder Using an Eye Tracking System
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8397136
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8397136
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ISSN
2077-0383
E-ISSN
2077-0383
DOI
10.3390/jcm10163541
