Sarcoglycanopathies: a multiplex molecular analysis for the most common mutations (2006)
Fonte: Diagnostic Molecular Pathology. Unidade: IB
Assuntos: DISTROFIA MUSCULAR, MUTAÇÃO GENÉTICA, GENÉTICA MÉDICA
ABNT
GOUVEIA, Telma Luciana Furtado et al. Sarcoglycanopathies: a multiplex molecular analysis for the most common mutations. Diagnostic Molecular Pathology, v. 15, n. ju 2006, p. 95-100, 2006Tradução . . Acesso em: 15 out. 2025.APA
Gouveia, T. L. F., Paim, J. F. O., Pavanello, R. de C. M., Zatz, M., & Vainzof, M. (2006). Sarcoglycanopathies: a multiplex molecular analysis for the most common mutations. Diagnostic Molecular Pathology, 15( ju 2006), 95-100.NLM
Gouveia TLF, Paim JFO, Pavanello R de CM, Zatz M, Vainzof M. Sarcoglycanopathies: a multiplex molecular analysis for the most common mutations. Diagnostic Molecular Pathology. 2006 ; 15( ju 2006): 95-100.[citado 2025 out. 15 ]Vancouver
Gouveia TLF, Paim JFO, Pavanello R de CM, Zatz M, Vainzof M. Sarcoglycanopathies: a multiplex molecular analysis for the most common mutations. Diagnostic Molecular Pathology. 2006 ; 15( ju 2006): 95-100.[citado 2025 out. 15 ]