Visual Function in Children with GNAO1-Related Encephalopathy
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DOI: 10.3390/genes14030544
Abstract: Background: GNAO1-related encephalopathies include a broad spectrum of developmental disorders caused by de novo heterozygous mutations in the GNAO1 gene, encoding the G (o) subunit α of G-proteins. These conditions are characterized by epilepsy, movement… read more here.
Keywords: function children; function; gnao1 related; children gnao1 ... See more keywords