APA (7th ed.) Citation

Herzog, A., Hartung, R., Reuser, A. J. J., Hermanns, P., Runz, H., Karabul, N., . . . Mengel, E. (2012). A cross-sectional single-centre study on the spectrum of Pompe disease, German patients: Molecular analysis of the GAA gene, manifestation and genotype-phenotype correlations. Orphanet Journal of Rare Diseases, 7(1), 35. https://doi.org/10.1186/1750-1172-7-35

Chicago Style (17th ed.) Citation

Herzog, Andreas, et al. "A Cross-sectional Single-centre Study on the Spectrum of Pompe Disease, German Patients: Molecular Analysis of the GAA Gene, Manifestation and Genotype-phenotype Correlations." Orphanet Journal of Rare Diseases 7, no. 1 (2012): 35. https://doi.org/10.1186/1750-1172-7-35.

MLA (9th ed.) Citation

Herzog, Andreas, et al. "A Cross-sectional Single-centre Study on the Spectrum of Pompe Disease, German Patients: Molecular Analysis of the GAA Gene, Manifestation and Genotype-phenotype Correlations." Orphanet Journal of Rare Diseases, vol. 7, no. 1, 2012, p. 35, https://doi.org/10.1186/1750-1172-7-35.