Recurrent LGMD2A (Calpainopathy) mutations in brazilian patients (2000)
Source: American Journal of Human Genetics. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
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PAULA, F et al. Recurrent LGMD2A (Calpainopathy) mutations in brazilian patients. American Journal of Human Genetics. Chicago: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 26 ago. 2024. , 2000APA
Paula, F., Moreira, E. S., Bernadino, A. L. F., Kai, A., Passos-Bueno, M. R., Vainzof, M., & Zatz, M. (2000). Recurrent LGMD2A (Calpainopathy) mutations in brazilian patients. American Journal of Human Genetics. Chicago: Instituto de Biociências, Universidade de São Paulo.NLM
Paula F, Moreira ES, Bernadino ALF, Kai A, Passos-Bueno MR, Vainzof M, Zatz M. Recurrent LGMD2A (Calpainopathy) mutations in brazilian patients. American Journal of Human Genetics. 2000 ; 67( 4): 251.[citado 2024 ago. 26 ]Vancouver
Paula F, Moreira ES, Bernadino ALF, Kai A, Passos-Bueno MR, Vainzof M, Zatz M. Recurrent LGMD2A (Calpainopathy) mutations in brazilian patients. American Journal of Human Genetics. 2000 ; 67( 4): 251.[citado 2024 ago. 26 ]