Source: Clinical rheumatology. Unidade: FM
Subjects: ANGIOGRAFIA, PROMOÇÃO DA SAÚDE, DOENÇAS CARDIOVASCULARES, TIROTROFINA, HORMÔNIOS DA ADENO-HIPÓFISE, FATORES DE RISCO
ABNT
SHINJO, Samuel Katsuyuki et al. A Brazilian family with inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia linked to the VCP pGly97Glu mutation. Clinical rheumatology, v. 37, n. 4, p. 1129-1136, 2018Tradução . . Disponível em: https://doi.org/10.1007/s10067-017-3913-1. Acesso em: 15 out. 2024.APA
Shinjo, S. K., Oba-shinjo, S. M., Lerario, A. M., & Marie, S. K. N. (2018). A Brazilian family with inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia linked to the VCP pGly97Glu mutation. Clinical rheumatology, 37( 4), 1129-1136. doi:10.1007/s10067-017-3913-1NLM
Shinjo SK, Oba-shinjo SM, Lerario AM, Marie SKN. A Brazilian family with inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia linked to the VCP pGly97Glu mutation [Internet]. Clinical rheumatology. 2018 ; 37( 4): 1129-1136.[citado 2024 out. 15 ] Available from: https://doi.org/10.1007/s10067-017-3913-1Vancouver
Shinjo SK, Oba-shinjo SM, Lerario AM, Marie SKN. A Brazilian family with inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia linked to the VCP pGly97Glu mutation [Internet]. Clinical rheumatology. 2018 ; 37( 4): 1129-1136.[citado 2024 out. 15 ] Available from: https://doi.org/10.1007/s10067-017-3913-1