Phenotypic diversity in an international Cure VCP Disease registry | Orphanet Journal of Rare Diseases | Full Text

Phenotypic diversity in an international Cure VCP Disease registry | Orphanet Journal of Rare Diseases | Full Text

1. Phenotypic diversity in an international Cure VCP Disease registry

   Dominant mutations in valosin-containing protein (VCP) gene cause an adult onset inclusion body myopathy, Paget’s disease of bone, and frontotemporal dementia also termed multisystem proteinopathy (MSP). The g...

   Authors:Chiseko Ikenaga, Andrew R. Findlay, Michelle Seiffert, Allison Peck, Nathan Peck, Nicholas E. Johnson, Jeffrey M. Statland and Conrad C. Weihl

   Citation:Orphanet Journal of Rare Diseases 2020 15:267

   Content type:Research

    

   Published on: 29 September 2020

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