Publication | Closed Access
The phenotype of Charcot–Marie–Tooth disease type 4C due to SH3TC2 mutations and possible predisposition to an inflammatory neuropathy
95
Citations
17
References
2009
Year
MedicinePathogenesisSh3tc2 MutationsPathologyDegenerative DiseaseNeurologyInflammatory NeuropathyPossible Predisposition
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