Fonte: Movement disorders clinical practice. Unidade: FM
Assuntos: FENÓTIPOS, BIOMARCADORES, DOENÇAS NEURODEGENERATIVAS, DOENÇAS CEREBRAIS
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PARMERA, Jacy Bezerra et al. Expanding MAPT p.V363I Mutation Phenotype: An Overlapping of PSP-CBS and Posterior Cortical Atrophy. Movement disorders clinical practice, v. 10, n. 4, p. 716-718, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/53947. Acesso em: 01 nov. 2024.APA
Parmera, J. B., Coutinho, A. M. N., Guimarães, T. G., Yamamoto, J. Y. S., Takada, L. T., Nitrini, R., et al. (2023). Expanding MAPT p.V363I Mutation Phenotype: An Overlapping of PSP-CBS and Posterior Cortical Atrophy. Movement disorders clinical practice, 10( 4), 716-718. doi:10.1002/mdc3.13671NLM
Parmera JB, Coutinho AMN, Guimarães TG, Yamamoto JYS, Takada LT, Nitrini R, Barbosa ER, Brucki SMD. Expanding MAPT p.V363I Mutation Phenotype: An Overlapping of PSP-CBS and Posterior Cortical Atrophy [Internet]. Movement disorders clinical practice. 2023 ; 10( 4): 716-718.[citado 2024 nov. 01 ] Available from: https://observatorio.fm.usp.br/handle/OPI/53947Vancouver
Parmera JB, Coutinho AMN, Guimarães TG, Yamamoto JYS, Takada LT, Nitrini R, Barbosa ER, Brucki SMD. Expanding MAPT p.V363I Mutation Phenotype: An Overlapping of PSP-CBS and Posterior Cortical Atrophy [Internet]. Movement disorders clinical practice. 2023 ; 10( 4): 716-718.[citado 2024 nov. 01 ] Available from: https://observatorio.fm.usp.br/handle/OPI/53947