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| Muscular dystrophy and myopathy_Paediatric v1.50 | FOXP3 | Bryony Thompson Marked gene: FOXP3 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Muscular dystrophy and myopathy_Paediatric v1.50 | FOXP3 | Bryony Thompson Gene: foxp3 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Muscular dystrophy and myopathy_Paediatric v1.50 | FOXP3 |
Bryony Thompson gene: FOXP3 was added gene: FOXP3 was added to Muscular dystrophy and myopathy_Paediatric. Sources: Literature Mode of inheritance for gene: FOXP3 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females Publications for gene: FOXP3 were set to 38982518 Phenotypes for gene: FOXP3 were set to congenital myopathy MONDO:0019952 Review for gene: FOXP3 was set to RED gene: FOXP3 was marked as current diagnostic Added comment: Single case reported with centronuclear myopathy. Sources: Literature |
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