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Filtros : "Bochow, Bettina" "Porta, Gilda" Removido: "Jacob, C. M. A." Limpar

Filtros

USP affiliated authors
- barbosa, egberto reis (~1)
- cancado, eduardo luiz rachid (~1)
- cançado, eduardo luiz rachid (~1)
- carrilho, flair josé (~1)
- porta, gilda (~1)
Date published
- 2004 (~1)
- 2002 (~1)
Subjects
- doenças degenerativas (genética) (1)
- doenças genéticas (diagnóstico) (1)
- fenótipos (1)
- gastroenterologia (1)
- genótipos (1)

Artigo de periodico
Wilson disease: novel mutations in the ATP7B gene and clinical correlation in Brazilian patients (2004)
Deguti, Marta M.; Genschel, Janine; Cançado, Eduardo L. R.; Barbosa, Egberto R.; Bochow, Bettina; Mucennic, Marcos; Porta, Gilda; Lochs, Herbert; Carrilho, Flair J.; Schmidt, Hartmut H.-J.
Source: Human mutation. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, FENÓTIPOS, GENÓTIPOS, DOENÇAS GENÉTICAS (DIAGNÓSTICO), DOENÇAS DEGENERATIVAS (GENÉTICA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DEGUTI, Marta M. et al. Wilson disease: novel mutations in the ATP7B gene and clinical correlation in Brazilian patients. Human mutation, v. 23, n. 4, p. online, 2004Tradução . . Disponível em: https://doi.org/10.1002/humu.9227. Acesso em: 10 ago. 2024.
APA
Deguti, M. M., Genschel, J., Cançado, E. L. R., Barbosa, E. R., Bochow, B., Mucennic, M., et al. (2004). Wilson disease: novel mutations in the ATP7B gene and clinical correlation in Brazilian patients. Human mutation, 23( 4), online. doi:10.1002/humu.9227
NLM
Deguti MM, Genschel J, Cançado ELR, Barbosa ER, Bochow B, Mucennic M, Porta G, Lochs H, Carrilho FJ, Schmidt HH-J. Wilson disease: novel mutations in the ATP7B gene and clinical correlation in Brazilian patients [Internet]. Human mutation. 2004 ; 23( 4): online.[citado 2024 ago. 10 ] Available from: https://doi.org/10.1002/humu.9227
Vancouver
Deguti MM, Genschel J, Cançado ELR, Barbosa ER, Bochow B, Mucennic M, Porta G, Lochs H, Carrilho FJ, Schmidt HH-J. Wilson disease: novel mutations in the ATP7B gene and clinical correlation in Brazilian patients [Internet]. Human mutation. 2004 ; 23( 4): online.[citado 2024 ago. 10 ] Available from: https://doi.org/10.1002/humu.9227
Trabalho de evento-resumo periodico
The Wilson disease gene mutation L708P in Brazil: a connection with the island of Gran Canaria ? (2002)
Deguti, Marta; Bochow, Bettina; Cancado, Eduardo L.; Barbosa, Egberto dos Reis; Genschel, Janine; Mucenic, Marcos; Porta, Gilda; Schmidt, Hartmut
Source: Hepatology/ Official Journal of the American for the Study of Liver Diseases. Conference titles: AASLD Annual Meeting and Postgraduate Courses. Unidade: FM
Subjects: HEPATOPATIAS, GASTROENTEROLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DEGUTI, Marta et al. The Wilson disease gene mutation L708P in Brazil: a connection with the island of Gran Canaria ?. Hepatology/ Official Journal of the American for the Study of Liver Diseases. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 10 ago. 2024. , 2002
APA
Deguti, M., Bochow, B., Cancado, E. L., Barbosa, E. dos R., Genschel, J., Mucenic, M., et al. (2002). The Wilson disease gene mutation L708P in Brazil: a connection with the island of Gran Canaria ? Hepatology/ Official Journal of the American for the Study of Liver Diseases. Philadelphia: Faculdade de Medicina, Universidade de São Paulo.
NLM
Deguti M, Bochow B, Cancado EL, Barbosa E dos R, Genschel J, Mucenic M, Porta G, Schmidt H. The Wilson disease gene mutation L708P in Brazil: a connection with the island of Gran Canaria ? Hepatology/ Official Journal of the American for the Study of Liver Diseases. 2002 ; 36( 4):[citado 2024 ago. 10 ]
Vancouver
Deguti M, Bochow B, Cancado EL, Barbosa E dos R, Genschel J, Mucenic M, Porta G, Schmidt H. The Wilson disease gene mutation L708P in Brazil: a connection with the island of Gran Canaria ? Hepatology/ Official Journal of the American for the Study of Liver Diseases. 2002 ; 36( 4):[citado 2024 ago. 10 ]

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