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...

Source: Orphanet Journal of Rare Diseases - September 29, 2020 Category: Internal Medicine Authors: Chiseko Ikenaga, Andrew R. Findlay, Michelle Seiffert, Allison Peck, Nathan Peck, Nicholas E. Johnson, Jeffrey M. Statland and Conrad C. Weihl Tags: Research Source Type: research