| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Muscular dystrophy and myopathy_Paediatric v0.166 | MYPN | Bryony Thompson Marked gene: MYPN as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Muscular dystrophy and myopathy_Paediatric v0.166 | MYPN | Bryony Thompson Gene: mypn has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Muscular dystrophy and myopathy_Paediatric v0.166 | MYPN | Bryony Thompson Classified gene: MYPN as Green List (high evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Muscular dystrophy and myopathy_Paediatric v0.166 | MYPN | Bryony Thompson Gene: mypn has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Muscular dystrophy and myopathy_Paediatric v0.128 | MYPN |
Sangavi Sivagnanasundram gene: MYPN was added gene: MYPN was added to Muscular dystrophy_Paediatric. Sources: Other Mode of inheritance for gene: MYPN was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: MYPN were set to 28017374 Phenotypes for gene: MYPN were set to Nemaline Myopathy (MIM#617336; MONDO:0018958) Review for gene: MYPN was set to GREEN Added comment: PMID: 28017374 Slowly progressive myopathy with onset in childhood Identified in at least 4 individuals Sources: Other |
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