APA (7th ed.) Citation

Genc, H. M., Ardicli, D., Haliloglu, G., Talim, B., Alikasifoglu, M., & Topaloglu, H. (2016). P.172 - Solving a puzzle: Incidentally detected high creatine kinase level combined with a family history of cardiomyopathy and sudden unexplained death leading to diagnosis of LMNA mutation. Neuromuscular Disorders, 26, S138. https://doi.org/10.1016/j.nmd.2016.06.192

Chicago Style (17th ed.) Citation

Genc, H. Maras, D. Ardicli, G. Haliloglu, B. Talim, M. Alikasifoglu, and H. Topaloglu. "P.172 - Solving a Puzzle: Incidentally Detected High Creatine Kinase Level Combined with a Family History of Cardiomyopathy and Sudden Unexplained Death Leading to Diagnosis of LMNA Mutation." Neuromuscular Disorders 26 (2016): S138. https://doi.org/10.1016/j.nmd.2016.06.192.

MLA (9th ed.) Citation

Genc, H. Maras, et al. "P.172 - Solving a Puzzle: Incidentally Detected High Creatine Kinase Level Combined with a Family History of Cardiomyopathy and Sudden Unexplained Death Leading to Diagnosis of LMNA Mutation." Neuromuscular Disorders, vol. 26, 2016, p. S138, https://doi.org/10.1016/j.nmd.2016.06.192.