Point mutation in a becker muscular dystrophy patient (1993)
Roberts, R G; Passos-Bueno, Maria Rita 
; Bobrow, M; Vainzof, Mariz ; Zatz, Mayana
Source: Human Molecular Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
ROBERTS, R G et al. Point mutation in a becker muscular dystrophy patient. Human Molecular Genetics, v. 2 , n. 1 , p. 75-7, 1993Tradução . . Disponível em: https://doi.org/10.1093/hmg/2.1.75. Acesso em: 12 out. 2024.APA
Roberts, R. G., Passos-Bueno, M. R., Bobrow, M., Vainzof, M., & Zatz, M. (1993). Point mutation in a becker muscular dystrophy patient. Human Molecular Genetics, 2 ( 1 ), 75-7. doi:10.1093/hmg/2.1.75NLM
Roberts RG, Passos-Bueno MR, Bobrow M, Vainzof M, Zatz M. Point mutation in a becker muscular dystrophy patient [Internet]. Human Molecular Genetics. 1993 ;2 ( 1 ): 75-7.[citado 2024 out. 12 ] Available from: https://doi.org/10.1093/hmg/2.1.75Vancouver
Roberts RG, Passos-Bueno MR, Bobrow M, Vainzof M, Zatz M. Point mutation in a becker muscular dystrophy patient [Internet]. Human Molecular Genetics. 1993 ;2 ( 1 ): 75-7.[citado 2024 out. 12 ] Available from: https://doi.org/10.1093/hmg/2.1.75
