One family, one gene and three phenotypes: A novel VCP (valosin-containing protein) mutation associated with myopathy with rimmed vacuoles, amyotrophic lateral sclerosis and frontotemporal dementia

Overview of attention for article published in Journal of the Neurological Sciences, July 2016

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One family, one gene and three phenotypes: A novel VCP (valosin-containing protein) mutation associated with myopa… https://t.co/1y0kfe4Kpm

RT @NeuroGen_papers: PubMed: One family, one gene and three phenotypes: A novel VCP (valosin-containing protein) mutation associated… https…

PubMed: One family, one gene and three phenotypes: A novel VCP (valosin-containing protein) mutation associated… https://t.co/vKBbTSf1VN

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