A FRET-based assay for characterization of alternative splicing events using peptide nucleic acid fluorescence in situ hybridization

por Blanco, Ana M., Rausell, Laura, Aguado, Begoña, Perez-Alonso, Manuel, Artero, Rubén
Publicado 2009

Novel intragenic deletion within the FXN gene in a patient with typical phenotype of Friedreich ataxia: may be more prevalent than we think?

por Aguilera, Cinthia, Esteve-Garcia, Anna, Casasnovas, Carlos, Vélez-Santamaria, Valentina, Rausell, Laura, Gargallo, Pablo, Garcia-Planells, Javier, Alía, Pedro, Llecha, Núria, Padró-Miquel, Ariadna
Publicado 2023