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Psychiatric Presentation of Frontotemporal Dementia Associated with Inclusion Body Myopathy due to the VCP Mutation (R155H) in a French Family
INTRODUCTION: Inclusion body myopathy with Paget's disease of the bone and frontotemporal dementia (IBMPFD) is a rare late-onset autosomal dominant disorder due to a mutation of the valosin-containing protein (VCP) gene. CASE REPORT: We report the case of a patient who developed progressive wea...
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Main Authors: | , , , , , , , , , |
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格式: | Artigo |
語言: | Inglês |
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S. Karger AG
2013
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在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3843933/ https://ncbi.nlm.nih.gov/pubmed/24348398 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000356481 |
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