Fanganiello, R. D.; Kimonis, V. E.; Nitrini, R.; Côrte, C. C.; Passos-Bueno, Maria Rita 
Source: Brazilian Journal of Medical and Biological Research. Unidades: FM, IB
Subjects: DEMÊNCIA (GENÉTICA), DOENÇAS HEREDITÁRIAS, MUTAÇÃO GENÉTICA, DOENÇAS ÓSSEAS
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FANGANIELLO, R. D. et al. A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia. Brazilian Journal of Medical and Biological Research, v. 44, n. 4, p. 374-380, 2011Tradução . . Disponível em: https://doi.org/10.1590/S0100-879X2011007500028. Acesso em: 30 abr. 2024.APA
Fanganiello, R. D., Kimonis, V. E., Nitrini, R., Côrte, C. C., & Passos-Bueno, M. R. (2011). A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia. Brazilian Journal of Medical and Biological Research, 44( 4), 374-380. doi:10.1590/S0100-879X2011007500028NLM
Fanganiello RD, Kimonis VE, Nitrini R, Côrte CC, Passos-Bueno MR. A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia [Internet]. Brazilian Journal of Medical and Biological Research. 2011 ; 44( 4): 374-380.[citado 2024 abr. 30 ] Available from: https://doi.org/10.1590/S0100-879X2011007500028Vancouver
Fanganiello RD, Kimonis VE, Nitrini R, Côrte CC, Passos-Bueno MR. A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia [Internet]. Brazilian Journal of Medical and Biological Research. 2011 ; 44( 4): 374-380.[citado 2024 abr. 30 ] Available from: https://doi.org/10.1590/S0100-879X2011007500028
