gamma-aminobutyric acid type A receptor alpha3 subunit
OMIM: 305660, Gene2Phenotype
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| GABRA3 in Mendeliome
                    
                    
                     | 1 review | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) | Sources
 Phenotypes
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| GABRA3 in Genetic Epilepsy
                    
                    
                       | 1 review | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) | Sources
 Phenotypes
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| GABRA3 in Intellectual disability syndromic and non-syndromic
                    
                    
                       | 1 review | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) | Sources
 Phenotypes
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