A Brazilian family with inclusion body myopathy associated with Paget’s disease of bone and frontotemporal dementia linked to the VCP pGly97Glu mutation
Crossref DOI link: https://doi.org/10.1007/s10067-017-3913-1
Published Online: 2017-11-10
Published Print: 2018-04
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Shinjo, Samuel Katsuyuki
Oba-Shinjo, Sueli Mieko
Lerario, Antonio Marcondes
Marie, Suely Kazue Nagahashi
License valid from 2017-11-10