Axonal hyperpolarization in inclusion-bo
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Kishore R. Kumar; Christina Liang; Merilee Needham; David Burke; Carolyn M. Sue;
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Article
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2011
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John Wiley and Sons
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English
⚖ 388 KB
👁 1 views
## Abstract ## Introduction: Inclusion‐body myopathy, Paget disease of the bone, and frontotemporal dementia (IBMPFD) is an autosomal dominant disorder due to mutations in the valosin‐containing protein (VCP) gene. Patients with this disorder may have neuropathic or myopathic features. ## Methods