Phenotypic diversity in an international Cure VCP Disease registry
Published 11 December 2020 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 genotype-phenotype relationships in VCP-related MSP are still being defined; in order to understand this better, we investigated the phenotypic diversity and pattern
https://www.lupop.lu.se/article/phenotypic-diversity-international-cure-vcp-disease-registry - 2025-04-27