A case of mitochondrial DNA depletion syndrome type 11-expanding the genotype and phenotype (2023)
Source: Neuromuscular disorders. Unidade: FM
Subjects: DNA MITOCONDRIAL, MIOPATIAS MITOCONDRIAIS, DOENÇAS RARAS
ABNT
ROCHA, Emanuelle Bianchi da Silva et al. A case of mitochondrial DNA depletion syndrome type 11-expanding the genotype and phenotype. Neuromuscular disorders, v. 33, n. 8, p. 692-696, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/57456. Acesso em: 18 ago. 2024.APA
Rocha, E. B. da S., Rodrigues, K. de L., Montouro, L. A. M., Coelho, E. N., Kouyoumdjian, J. A., Kok, F., et al. (2023). A case of mitochondrial DNA depletion syndrome type 11-expanding the genotype and phenotype. Neuromuscular disorders, 33( 8), 692-696. doi:10.1016/j.nmd.2023.06.004NLM
Rocha EB da S, Rodrigues K de L, Montouro LAM, Coelho EN, Kouyoumdjian JA, Kok F, Nobrega PR, Graca CR, Morita M da PA, Estephan E de P. A case of mitochondrial DNA depletion syndrome type 11-expanding the genotype and phenotype [Internet]. Neuromuscular disorders. 2023 ; 33( 8): 692-696.[citado 2024 ago. 18 ] Available from: https://observatorio.fm.usp.br/handle/OPI/57456Vancouver
Rocha EB da S, Rodrigues K de L, Montouro LAM, Coelho EN, Kouyoumdjian JA, Kok F, Nobrega PR, Graca CR, Morita M da PA, Estephan E de P. A case of mitochondrial DNA depletion syndrome type 11-expanding the genotype and phenotype [Internet]. Neuromuscular disorders. 2023 ; 33( 8): 692-696.[citado 2024 ago. 18 ] Available from: https://observatorio.fm.usp.br/handle/OPI/57456