Garcia-Diaz, Beatriz; Barros, Mário Henrique de 
; Sanna-Cherchi, Simone; Emmanuele, Valentina; Akman, Hasan O.; Ferreiro-Barros, Claudia C.; Horvath, Rita; Tadesse, Saba; El Gharaby, Nader; Di Mauro, Salvatore; De Vivo, Darryl C.; Shokr, Aly; Hirano, Michio; Quinzii, Catarina M.
Source: American Journal of Human Genetics. Unidade: ICB
Assunto: MICROBIOLOGIA
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ABNT
GARCIA-DIAZ, Beatriz et al. Infantile encephaloneuromyopathy and defective mitochondrial translation are due to a homozygous RMND1 mutation. American Journal of Human Genetics, v. 91, n. 4, p. 729-736, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.ajhg.2012.08.019. Acesso em: 01 nov. 2024.APA
Garcia-Diaz, B., Barros, M. H. de, Sanna-Cherchi, S., Emmanuele, V., Akman, H. O., Ferreiro-Barros, C. C., et al. (2012). Infantile encephaloneuromyopathy and defective mitochondrial translation are due to a homozygous RMND1 mutation. American Journal of Human Genetics, 91( 4), 729-736. doi:10.1016/j.ajhg.2012.08.019NLM
Garcia-Diaz B, Barros MH de, Sanna-Cherchi S, Emmanuele V, Akman HO, Ferreiro-Barros CC, Horvath R, Tadesse S, El Gharaby N, Di Mauro S, De Vivo DC, Shokr A, Hirano M, Quinzii CM. Infantile encephaloneuromyopathy and defective mitochondrial translation are due to a homozygous RMND1 mutation [Internet]. American Journal of Human Genetics. 2012 ; 91( 4): 729-736.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.ajhg.2012.08.019Vancouver
Garcia-Diaz B, Barros MH de, Sanna-Cherchi S, Emmanuele V, Akman HO, Ferreiro-Barros CC, Horvath R, Tadesse S, El Gharaby N, Di Mauro S, De Vivo DC, Shokr A, Hirano M, Quinzii CM. Infantile encephaloneuromyopathy and defective mitochondrial translation are due to a homozygous RMND1 mutation [Internet]. American Journal of Human Genetics. 2012 ; 91( 4): 729-736.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.ajhg.2012.08.019
