The limb-girdle muscular dystrophy 2G (LGMD2G) phenotype (2000)
- Authors:
- USP affiliated authors: MARIE, SUELY KAZUE NAGAHASHI - FM ; ZATZ, MAYANA - IB ; BUENO, MARIA RITA DOS SANTOS E PASSOS - IB
- Unidades: FM; IB
- Assunto: NEUROLOGIA
- Language: Inglês
- Imprenta:
- Publisher place: Kidlington Oxford
- Date published: 2000
- Source:
- Título: Neuromuscular Disorders
- Volume/Número/Paginação/Ano: v. 10, n. 4-5, p. 346, June 2000
- Conference titles: International Congress of the World Muscle Society
-
ABNT
PASSOS-BUENO, Maria Rita et al. The limb-girdle muscular dystrophy 2G (LGMD2G) phenotype. Neuromuscular Disorders. Kidlington Oxford: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 28 dez. 2025. , 2000 -
APA
Passos-Bueno, M. R., De Sá Moreira, E., Marie, S. K. N., Pavanello, R. C. M., Zanoteli, E., Vainzof, M., & Zatz, M. (2000). The limb-girdle muscular dystrophy 2G (LGMD2G) phenotype. Neuromuscular Disorders. Kidlington Oxford: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Passos-Bueno MR, De Sá Moreira E, Marie SKN, Pavanello RCM, Zanoteli E, Vainzof M, Zatz M. The limb-girdle muscular dystrophy 2G (LGMD2G) phenotype. Neuromuscular Disorders. 2000 ; 10( 4-5): 346.[citado 2025 dez. 28 ] -
Vancouver
Passos-Bueno MR, De Sá Moreira E, Marie SKN, Pavanello RCM, Zanoteli E, Vainzof M, Zatz M. The limb-girdle muscular dystrophy 2G (LGMD2G) phenotype. Neuromuscular Disorders. 2000 ; 10( 4-5): 346.[citado 2025 dez. 28 ] - Estudo molecular de neuropatias periféricas - CMT1A e HNPP
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