載入...
Phenotypic variability in three families with valosin-containing protein mutation
BACKGROUND AND PURPOSE: The phenotype of IBMPFD [inclusion body myopathy with Paget’s disease of the bone and frontotemporal dementia (FTD)] associated with valosin-containing protein(VCP) mutation is described in three families. METHODS: Probands were identified based on a pathological diagnosis of...
Na minha lista:
Main Authors: | , , , , , , , , , , |
---|---|
格式: | Artigo |
語言: | Inglês |
出版: |
2012
|
主題: | |
在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3734548/ https://ncbi.nlm.nih.gov/pubmed/22900631 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1468-1331.2012.03831.x |
標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|