Source: Neuromuscular Disorders. Conference titles: International Congress of the World Muscle Society. Unidade: IB
Subjects: DISTROFIA MUSCULAR (CONGRESSOS), DOENÇAS GENÉTICAS (CONGRESSOS)
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ABNT
FROSK, P. et al. The most common mutation in FKRP causing limb girdle muscular dystrophy type 21 (LGMD21) may have occured only once. Neuromuscular Disorders. Oxford: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 02 out. 2024. , 2004APA
Frosk, P., Bushby, K., Zatz, M., Straub, V., Greenberg, C. R., & Wrogemann, K. (2004). The most common mutation in FKRP causing limb girdle muscular dystrophy type 21 (LGMD21) may have occured only once. Neuromuscular Disorders. Oxford: Instituto de Biociências, Universidade de São Paulo.NLM
Frosk P, Bushby K, Zatz M, Straub V, Greenberg CR, Wrogemann K. The most common mutation in FKRP causing limb girdle muscular dystrophy type 21 (LGMD21) may have occured only once. Neuromuscular Disorders. 2004 ; 14( 8-9): 579.[citado 2024 out. 02 ]Vancouver
Frosk P, Bushby K, Zatz M, Straub V, Greenberg CR, Wrogemann K. The most common mutation in FKRP causing limb girdle muscular dystrophy type 21 (LGMD21) may have occured only once. Neuromuscular Disorders. 2004 ; 14( 8-9): 579.[citado 2024 out. 02 ]