APA

Alías L., Bernal S., Fuentes-Prior P., Barceló M. J., Also E., Martínez-Hernández R., Rodríguez-Alvarez F. J., Martín Y., Aller E., Grau E., Peciña A., Antiñolo G., Galán E., Rosa A. L., Fernández-Burriel M., Borrego S., Millán J. M., Hernández-Chico C., Baiget M. & Tizzano E. F. (20090202). Mutation update of spinal muscular atrophy in Spain: molecular characterization of 745 unrelated patients and identification of four novel mutations in the SMN1 gene. : Human genetics.

Chicago

Alías Laura, Bernal Sara, Fuentes-Prior Pablo, Barceló María Jesus, Also Eva, Martínez-Hernández Rebeca, Rodríguez-Alvarez Francisco J, Martín Yolanda, Aller Elena, Grau Elena, Peciña Ana, Antiñolo Guillermo, Galán Enrique, Rosa Alberto L, Fernández-Burriel Miguel, Borrego Salud, Millán José M, Hernández-Chico Concepción, Baiget Montserrat and Tizzano Eduardo F. 20090202. Mutation update of spinal muscular atrophy in Spain: molecular characterization of 745 unrelated patients and identification of four novel mutations in the SMN1 gene. : Human genetics.

Harvard

Alías L., Bernal S., Fuentes-Prior P., Barceló M. J., Also E., Martínez-Hernández R., Rodríguez-Alvarez F. J., Martín Y., Aller E., Grau E., Peciña A., Antiñolo G., Galán E., Rosa A. L., Fernández-Burriel M., Borrego S., Millán J. M., Hernández-Chico C., Baiget M. and Tizzano E. F. (20090202). Mutation update of spinal muscular atrophy in Spain: molecular characterization of 745 unrelated patients and identification of four novel mutations in the SMN1 gene. : Human genetics.

MLA

Alías Laura, Bernal Sara, Fuentes-Prior Pablo, Barceló María Jesus, Also Eva, Martínez-Hernández Rebeca, Rodríguez-Alvarez Francisco J, Martín Yolanda, Aller Elena, Grau Elena, Peciña Ana, Antiñolo Guillermo, Galán Enrique, Rosa Alberto L, Fernández-Burriel Miguel, Borrego Salud, Millán José M, Hernández-Chico Concepción, Baiget Montserrat and Tizzano Eduardo F. Mutation update of spinal muscular atrophy in Spain: molecular characterization of 745 unrelated patients and identification of four novel mutations in the SMN1 gene. : Human genetics. 20090202.