APA (7th ed.) Citation

Garibaldi, M., Fattori, F., Bortolotti, C., Brochier, G., Labasse, C., Verardo, M., . . . Antonini, G. (2018). CONGENITAL MYOPATHIES: NEMALINE AND TITINOPATHIES: P.232Core and rod myopathy due to a novel mutation in BTB domain of KBTBD13 gene presenting as LGMD. Neuromuscular Disorders, 28, S102. https://doi.org/10.1016/j.nmd.2018.06.280

Chicago Style (17th ed.) Citation

Garibaldi, M., et al. "CONGENITAL MYOPATHIES: NEMALINE AND TITINOPATHIES: P.232Core and Rod Myopathy Due to a Novel Mutation in BTB Domain of KBTBD13 Gene Presenting as LGMD." Neuromuscular Disorders 28 (2018): S102. https://doi.org/10.1016/j.nmd.2018.06.280.

MLA (9th ed.) Citation

Garibaldi, M., et al. "CONGENITAL MYOPATHIES: NEMALINE AND TITINOPATHIES: P.232Core and Rod Myopathy Due to a Novel Mutation in BTB Domain of KBTBD13 Gene Presenting as LGMD." Neuromuscular Disorders, vol. 28, 2018, p. S102, https://doi.org/10.1016/j.nmd.2018.06.280.