A Unique Myopathy Syndrome in a Patient Disclosing Clinical, Laboratory, and Genetic Findings of Late-Onset Pompe Disease, Together with a Lack of Dysferlin on Muscle Biopsy

MLA

Sampaolo, Simone, et al. “A Unique Myopathy Syndrome in a Patient Disclosing Clinical, Laboratory, and Genetic Findings of Late-Onset Pompe Disease, Together with a Lack of Dysferlin on Muscle Biopsy.” Journal of Neuromuscular Diseases, vol. 2, no. 1, Jan. 2015, pp. S29–30. EBSCOhost, https://doi.org/10.3233/JND-159027.

APA

Sampaolo, S., Lombardi, L., Pascarella, A., Picillo, E., Farina, O., Esposito, T., Politano, L., & Di Iorio, G. (2015). A Unique Myopathy Syndrome in a Patient Disclosing Clinical, Laboratory, and Genetic Findings of Late-Onset Pompe Disease, Together with a Lack of Dysferlin on Muscle Biopsy. Journal of Neuromuscular Diseases, 2(1), S29–S30. https://doi.org/10.3233/JND-159027

Chicago

Sampaolo, Simone, Luca Lombardi, Angelo Pascarella, Esther Picillo, Olimpia Farina, Teresa Esposito, Luisa Politano, and Giuseppe Di Iorio. 2015. “A Unique Myopathy Syndrome in a Patient Disclosing Clinical, Laboratory, and Genetic Findings of Late-Onset Pompe Disease, Together with a Lack of Dysferlin on Muscle Biopsy.” Journal of Neuromuscular Diseases 2 (1): S29–30. doi:10.3233/JND-159027.