| Human Disease |
Myopathy, Centronuclear, 1; CNM1 OMIM ID: 160150 |
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| Synonyms | Myopathy, Centronuclear, Autosomal Dominant; Myotubular Myopathy, Autosomal Dominant | |||||||||||||||||||||||||
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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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