Detection of variants in dystroglycanopathy-associated genes through the application of targeted whole-exome sequencing analysis to a large cohort of patients with unexplained limb-girdle muscle weakness

MLA

Katherine Johnson, et al. “Detection of Variants in Dystroglycanopathy-Associated Genes through the Application of Targeted Whole-Exome Sequencing Analysis to a Large Cohort of Patients with Unexplained Limb-Girdle Muscle Weakness.” Skeletal Muscle, vol. 8, no. 1, July 2018, pp. 1–12. EBSCOhost, https://doi.org/10.1186/s13395-018-0170-1.

APA

Katherine Johnson, Marta Bertoli, Lauren Phillips, Ana Töpf, Peter Van den Bergh, John Vissing, Nanna Witting, Shahriar Nafissi, Shirin Jamal-Omidi, Anna Łusakowska, Anna Kostera-Pruszczyk, Anna Potulska-Chromik, Nicolas Deconinck, Carina Wallgren-Pettersson, Sonja Strang-Karlsson, Jaume Colomer, Kristl G. Claeys, Willem De Ridder, Jonathan Baets, … Volker Straub. (2018). Detection of variants in dystroglycanopathy-associated genes through the application of targeted whole-exome sequencing analysis to a large cohort of patients with unexplained limb-girdle muscle weakness. Skeletal Muscle, 8(1), 1–12. https://doi.org/10.1186/s13395-018-0170-1

Chicago

Katherine Johnson, Marta Bertoli, Lauren Phillips, Ana Töpf, Peter Van den Bergh, John Vissing, Nanna Witting, et al. 2018. “Detection of Variants in Dystroglycanopathy-Associated Genes through the Application of Targeted Whole-Exome Sequencing Analysis to a Large Cohort of Patients with Unexplained Limb-Girdle Muscle Weakness.” Skeletal Muscle 8 (1): 1–12. doi:10.1186/s13395-018-0170-1.