| Human Disease |
Myasthenic Syndrome, Congenital, Fast-Channel OMIM ID: 608930 |
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| Synonyms | FCCMS | |||||||||||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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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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