Margutti, Ana Vitoria Barban; Silva Junior, Wilson Araújo da 
; Garcia, Daniel Fantozzi; Molfetta, Greice Andreotti de ; Marques, Adriana Aparecida; Amorim, Tatiana; Prazeres, Vânia Mesquita Gadelha; Silva, Raquel Tavares Boy da; Miura, Irene Kazue; Seda Neto, Joao; Santos, Emerson de Santana; Santos, Mara Lúcia Schmitz Ferreira; Lourenço, Charles Marques; Tonon, Tássia; Sperb-ludwig, Fernanda; Souza, Carolina Fischinger Moura de; Schwartz, Ida Vanessa Döederlein; Camelo Júnior, José Simon
Source: Orphanet Journal of Rare Diseases. Unidade: FMRP
Subjects: AMINOÁCIDOS, ERROS INATOS DO METABOLISMO, DOENÇA DA URINA DE XAROPE DE BORDO
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MARGUTTI, Ana Vitoria Barban et al. Maple syrup urine disease in Brazilian patients: variants and clinical phenotype heterogeneity. Orphanet Journal of Rare Diseases, v. 15, 2020Tradução . . Disponível em: https://doi.org/10.1186/s13023-020-01590-7. Acesso em: 04 nov. 2024.APA
Margutti, A. V. B., Silva Junior, W. A. da, Garcia, D. F., Molfetta, G. A. de, Marques, A. A., Amorim, T., et al. (2020). Maple syrup urine disease in Brazilian patients: variants and clinical phenotype heterogeneity. Orphanet Journal of Rare Diseases, 15. doi:10.1186/s13023-020-01590-7NLM
Margutti AVB, Silva Junior WA da, Garcia DF, Molfetta GA de, Marques AA, Amorim T, Prazeres VMG, Silva RTB da, Miura IK, Seda Neto J, Santos E de S, Santos MLSF, Lourenço CM, Tonon T, Sperb-ludwig F, Souza CFM de, Schwartz IVD, Camelo Júnior JS. Maple syrup urine disease in Brazilian patients: variants and clinical phenotype heterogeneity [Internet]. Orphanet Journal of Rare Diseases. 2020 ; 15[citado 2024 nov. 04 ] Available from: https://doi.org/10.1186/s13023-020-01590-7Vancouver
Margutti AVB, Silva Junior WA da, Garcia DF, Molfetta GA de, Marques AA, Amorim T, Prazeres VMG, Silva RTB da, Miura IK, Seda Neto J, Santos E de S, Santos MLSF, Lourenço CM, Tonon T, Sperb-ludwig F, Souza CFM de, Schwartz IVD, Camelo Júnior JS. Maple syrup urine disease in Brazilian patients: variants and clinical phenotype heterogeneity [Internet]. Orphanet Journal of Rare Diseases. 2020 ; 15[citado 2024 nov. 04 ] Available from: https://doi.org/10.1186/s13023-020-01590-7
