APA (7th ed.) Citation

Al-Maraghi, A., Shaath, R., Ford, K., Aamer, W., AlRayahi, J., Hussein, S., . . . Fakhro, K. A. (2025). Biallelic Loss-of-Function Variant in MINPP1 Causes Pontocerebellar Hypoplasia with Characteristic Severe Neurodevelopmental Disorder. International Journal of Molecular Sciences, 26(11), 5213. https://doi.org/10.3390/ijms26115213

Chicago Style (17th ed.) Citation

Al-Maraghi, Aljazi, et al. "Biallelic Loss-of-Function Variant in MINPP1 Causes Pontocerebellar Hypoplasia with Characteristic Severe Neurodevelopmental Disorder." International Journal of Molecular Sciences 26, no. 11 (2025): 5213. https://doi.org/10.3390/ijms26115213.

MLA (9th ed.) Citation

Al-Maraghi, Aljazi, et al. "Biallelic Loss-of-Function Variant in MINPP1 Causes Pontocerebellar Hypoplasia with Characteristic Severe Neurodevelopmental Disorder." International Journal of Molecular Sciences, vol. 26, no. 11, 2025, p. 5213, https://doi.org/10.3390/ijms26115213.