APA (7th ed.) Citation

Lerat, J., Cintas, P., Beauvais‐Dzugan, H., Magdelaine, C., Sturtz, F., & Lia, A. (2017). A complex homozygous mutation in ABHD12 responsible for PHARC syndrome discovered with NGS and review of the literature. Journal of the Peripheral Nervous System, 22(2), 77. https://doi.org/10.1111/jns.12216

Chicago Style (17th ed.) Citation

Lerat, Justine, Pascal Cintas, Hélène Beauvais‐Dzugan, Corinne Magdelaine, Franck Sturtz, and Anne‐Sophie Lia. "A Complex Homozygous Mutation in ABHD12 Responsible for PHARC Syndrome Discovered with NGS and Review of the Literature." Journal of the Peripheral Nervous System 22, no. 2 (2017): 77. https://doi.org/10.1111/jns.12216.

MLA (9th ed.) Citation

Lerat, Justine, et al. "A Complex Homozygous Mutation in ABHD12 Responsible for PHARC Syndrome Discovered with NGS and Review of the Literature." Journal of the Peripheral Nervous System, vol. 22, no. 2, 2017, p. 77, https://doi.org/10.1111/jns.12216.