Source: Abstracts. Conference titles: Annual Meeting of Pediatric Academic Societies. Unidade: FMRP
Subjects: ERROS INATOS DO METABOLISMO, ENZIMAS (DEFICIÊNCIA), MUTAÇÃO GENÉTICA
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CAMELO JUNIOR, Jose Simon e GARCIA, Daniel Fantozzi e SILVA JÚNIOR, Wilson Araújo da. Clinical and molecular characterization of classical galactosemia in Brazil with identification of six novel mutations. 2013, Anais.. Washington: PAS, 2013. . Acesso em: 10 nov. 2024.APA
Camelo Junior, J. S., Garcia, D. F., & Silva Júnior, W. A. da. (2013). Clinical and molecular characterization of classical galactosemia in Brazil with identification of six novel mutations. In Abstracts. Washington: PAS.NLM
Camelo Junior JS, Garcia DF, Silva Júnior WA da. Clinical and molecular characterization of classical galactosemia in Brazil with identification of six novel mutations. Abstracts. 2013 ;[citado 2024 nov. 10 ]Vancouver
Camelo Junior JS, Garcia DF, Silva Júnior WA da. Clinical and molecular characterization of classical galactosemia in Brazil with identification of six novel mutations. Abstracts. 2013 ;[citado 2024 nov. 10 ]
