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| Neurotransmitter Defects v2.0 | GABRB2 | Gene migrated from ENSG00000145864 to ENSG00000145864 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Neurotransmitter Defects v1.7 | GABRB2 |
Bryony Thompson gene: GABRB2 was added gene: GABRB2 was added to Neurotransmitter Defects. Sources: Expert Review Green Mode of inheritance for gene: GABRB2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: GABRB2 were set to 27789573; 35850019; 29100083 Phenotypes for gene: GABRB2 were set to Epileptic encephalopathy, infantile or early childhood, 2 MONDO:0020631; Gamma-aminobutyric acid neurotransmitter disorders |
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