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Gene Information
Gene symbol: FRAXE
Gene name: fragile site, folic acid type, rare, fra(X)(q28) E
HGNC ID: 3949
Related Genes
| # | Gene Symbol | Number of hits |
| 1 | FXN | 1 hits |
| 2 | FXR1 | 1 hits |
Related Sentences
| # | PMID | Sentence |
| 1 | 14526165 | Transcription defects induced by repeat expansion: fragile X syndrome, FRAXE mental retardation, progressive myoclonus epilepsy type 1, and Friedreich ataxia. |
| 2 | 14526165 | Fragile X mental retardation syndrome, FRAXE mental retardation, Progressive myoclonus epilepsy Type I, and Friedreich ataxia are members of a larger group of genetic disorders known as the Repeat Expansion Diseases. |
| 3 | 14526165 | Transcription defects induced by repeat expansion: fragile X syndrome, FRAXE mental retardation, progressive myoclonus epilepsy type 1, and Friedreich ataxia. |
| 4 | 14526165 | Fragile X mental retardation syndrome, FRAXE mental retardation, Progressive myoclonus epilepsy Type I, and Friedreich ataxia are members of a larger group of genetic disorders known as the Repeat Expansion Diseases. |