Compound heterozygosity for an expanded (GAA) and a (GAAGGA) repeat at FXN locus: from a diagnostic pitfall to potential clues to the pathogenesis of Friedreich ataxia

MLA

Vittorio Riso, et al. “Compound Heterozygosity for an Expanded (GAA) and a (GAAGGA) Repeat at FXN Locus: From a Diagnostic Pitfall to Potential Clues to the Pathogenesis of Friedreich Ataxia.” Neurogenetics, vol. 21, July 2020, pp. 279–87. EBSCOhost, https://doi.org/10.1007/s10048-020-00620-7.

APA

Vittorio Riso, Piergiorgio La Rosa, Massimo Santoro, Gabriella Silvestri, Pietro Chiurazzi, Fiorella Piemonte, Salvatore Rossi, Maria Grazia Pomponi, Tommaso Nicoletti, Sara Petrillo, Alessia Perna, & Anna Modoni. (2020). Compound heterozygosity for an expanded (GAA) and a (GAAGGA) repeat at FXN locus: from a diagnostic pitfall to potential clues to the pathogenesis of Friedreich ataxia. Neurogenetics, 21, 279–287. https://doi.org/10.1007/s10048-020-00620-7

Chicago

Vittorio Riso, Piergiorgio La Rosa, Massimo Santoro, Gabriella Silvestri, Pietro Chiurazzi, Fiorella Piemonte, Salvatore Rossi, et al. 2020. “Compound Heterozygosity for an Expanded (GAA) and a (GAAGGA) Repeat at FXN Locus: From a Diagnostic Pitfall to Potential Clues to the Pathogenesis of Friedreich Ataxia.” Neurogenetics 21 (July): 279–87. doi:10.1007/s10048-020-00620-7.