| Human Disease |
Charcot-Marie-Tooth Disease, Axonal, Type 2B; CMT2B OMIM ID: 600882 |
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| Synonyms | Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2B; Charcot-Marie-Tooth Neuropathy, Type 2B; Hereditary Motor and Sensory Neuropathy IIB; HMSN IIB; HMSN2B | |||||||||||||||||||||
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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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