Source: BMC Medical Genetics. Unidade: FM
Subjects: GLICOGENOSE, MUTAÇÃO GENÉTICA (ENZIMOLOGIA), CRIANÇAS
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SOGGIA, Ana Priscila et al. A novel mutation in the glycogen synthase 2 gene in a child with glycogen storage disease type 0. BMC Medical Genetics, v. 11, n. 3, p. 1-5, 2010Tradução . . Disponível em: https://doi.org/10.1186/1471-2350-11-3. Acesso em: 12 set. 2024.APA
Soggia, A. P., Correa-Giannella, M. L., Fortes, M. A. H., Luna, A. M. C., & Pereira, M. A. A. (2010). A novel mutation in the glycogen synthase 2 gene in a child with glycogen storage disease type 0. BMC Medical Genetics, 11( 3), 1-5. doi:10.1186/1471-2350-11-3NLM
Soggia AP, Correa-Giannella ML, Fortes MAH, Luna AMC, Pereira MAA. A novel mutation in the glycogen synthase 2 gene in a child with glycogen storage disease type 0 [Internet]. BMC Medical Genetics. 2010 ; 11( 3): 1-5.[citado 2024 set. 12 ] Available from: https://doi.org/10.1186/1471-2350-11-3Vancouver
Soggia AP, Correa-Giannella ML, Fortes MAH, Luna AMC, Pereira MAA. A novel mutation in the glycogen synthase 2 gene in a child with glycogen storage disease type 0 [Internet]. BMC Medical Genetics. 2010 ; 11( 3): 1-5.[citado 2024 set. 12 ] Available from: https://doi.org/10.1186/1471-2350-11-3