Sarcoglycanopathies: a multiplex molecular analysis for the most common mutations (2006)
- Authors:
- USP affiliated authors: ZATZ, MAYANA - IB ; VAINZOF, MARIZ - IB
- Unidade: IB
- Subjects: DISTROFIA MUSCULAR; MUTAÇÃO GENÉTICA; GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Publisher place: Hagerstown
- Date published: 2006
- Source:
- Título: Diagnostic Molecular Pathology
- ISSN: 1052-9551
- Volume/Número/Paginação/Ano: v. 15, n. 2, p. 95-100, jun. 2006
-
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: 06 nov. 2024. -
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 2024 nov. 06 ] -
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 2024 nov. 06 ] - Protein defects in neuromuscular diseases
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