Recurrent basque and brailian mutation in LGMD2A (Calpainopathy) brazilian families (2001)
Fonte: European Journal of Human Genetics. Nome do evento: International Congress of Human Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
ABNT
PAULA, Flavia de et al. Recurrent basque and brailian mutation in LGMD2A (Calpainopathy) brazilian families. European Journal of Human Genetics. Basingstoke: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 27 ago. 2024. , 2001APA
Paula, F. de, Viegas, R., Kai, A., Moreira, E. S., Passos-Bueno, M. R., Vainzof, M., et al. (2001). Recurrent basque and brailian mutation in LGMD2A (Calpainopathy) brazilian families. European Journal of Human Genetics. Basingstoke: Instituto de Biociências, Universidade de São Paulo.NLM
Paula F de, Viegas R, Kai A, Moreira ES, Passos-Bueno MR, Vainzof M, Nigro V, Zatz M. Recurrent basque and brailian mutation in LGMD2A (Calpainopathy) brazilian families. European Journal of Human Genetics. 2001 ; 9 396.[citado 2024 ago. 27 ]Vancouver
Paula F de, Viegas R, Kai A, Moreira ES, Passos-Bueno MR, Vainzof M, Nigro V, Zatz M. Recurrent basque and brailian mutation in LGMD2A (Calpainopathy) brazilian families. European Journal of Human Genetics. 2001 ; 9 396.[citado 2024 ago. 27 ]