APA (7th ed.) Citation

Srinivasan, V. M., Nilay, M., & Manisha, R. (2026). Primary Coenzyme Q10 Deficiency Type 7: A Potentially Treatable Cause of Developmental Delay. Neurology India, 74(3), 526. https://doi.org/10.4103/neurol-india.Neurol-India-D-25-00416

Chicago Style (17th ed.) Citation

Srinivasan, Varunvenkat M., Mayank Nilay, and Rani Manisha. "Primary Coenzyme Q10 Deficiency Type 7: A Potentially Treatable Cause of Developmental Delay." Neurology India 74, no. 3 (2026): 526. https://doi.org/10.4103/neurol-india.Neurol-India-D-25-00416.

MLA (9th ed.) Citation

Srinivasan, Varunvenkat M., et al. "Primary Coenzyme Q10 Deficiency Type 7: A Potentially Treatable Cause of Developmental Delay." Neurology India, vol. 74, no. 3, 2026, p. 526, https://doi.org/10.4103/neurol-india.Neurol-India-D-25-00416.

Warning: These citations may not always be 100% accurate.