Source: PLOS ONE. Unidade: FMRP
Subjects: TRANSFECÇÃO, REAÇÃO EM CADEIA POR POLIMERASE, DELEÇÃO DE GENES, MUTAÇÃO GENÉTICA, LISOSSOMOS, DOENÇAS NEURODEGENERATIVAS
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ZAMPIERI, Stefania et al. Sequence and copy number analyses of HEXB gene in patients affected by Sandhoff Disease: functional characterization of 9 novel sequence variants. PLOS ONE, v. 7, n. 7, p. 1-10, 2012Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0041516. Acesso em: 16 nov. 2024.APA
Zampieri, S., Cattarossi, S., Oller Ramirez, A. M., Rosano, C., Lourenço, C. M., Passon, N., et al. (2012). Sequence and copy number analyses of HEXB gene in patients affected by Sandhoff Disease: functional characterization of 9 novel sequence variants. PLOS ONE, 7( 7), 1-10. doi:10.1371/journal.pone.0041516NLM
Zampieri S, Cattarossi S, Oller Ramirez AM, Rosano C, Lourenço CM, Passon N, Moroni I, Uziel G, Pettinari A, Stanzial F, Kremer RD de, Azar NB, Hazan F, Filocamo M, Bembi B, Dardis A. Sequence and copy number analyses of HEXB gene in patients affected by Sandhoff Disease: functional characterization of 9 novel sequence variants [Internet]. PLOS ONE. 2012 ; 7( 7): 1-10.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1371/journal.pone.0041516Vancouver
Zampieri S, Cattarossi S, Oller Ramirez AM, Rosano C, Lourenço CM, Passon N, Moroni I, Uziel G, Pettinari A, Stanzial F, Kremer RD de, Azar NB, Hazan F, Filocamo M, Bembi B, Dardis A. Sequence and copy number analyses of HEXB gene in patients affected by Sandhoff Disease: functional characterization of 9 novel sequence variants [Internet]. PLOS ONE. 2012 ; 7( 7): 1-10.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1371/journal.pone.0041516
