| Human Disease |
Myasthenia, Limb-Girdle, Familial OMIM ID: 254300 |
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| Synonyms | Cms IB; Congenital Myasthenic Syndrome Type IB; CMS1B; LGM; Myasthenic Myopathy, Formerly | ||||||||||||||||||||||||||||
| View all models | View ALL (1) mouse models for this human disease. | ||||||||||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Agrnnmf380/Agrnnmf380 |
C57BL/6J-Agrnnmf380/J | J:176117 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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