Hashem, S.; Elhag, S.F.; Bhat, A.A.; Aamer, W.; Al-Maraghi, A.; Alhaboub, H.; Abuthaher, D.; Akil, A.S.A.-S.; Haris, M.; Fakhro, K.;
et al. Functional Interpretation of a Novel Homozygous METTL5 Variant Associated with ADHD and Neurodevelopmental Abnormalities: A Case Report and Literature Review. Genes 2025, 16, 1502.
https://doi.org/10.3390/genes16121502
AMA Style
Hashem S, Elhag SF, Bhat AA, Aamer W, Al-Maraghi A, Alhaboub H, Abuthaher D, Akil ASA-S, Haris M, Fakhro K,
et al. Functional Interpretation of a Novel Homozygous METTL5 Variant Associated with ADHD and Neurodevelopmental Abnormalities: A Case Report and Literature Review. Genes. 2025; 16(12):1502.
https://doi.org/10.3390/genes16121502
Chicago/Turabian Style
Hashem, Sheema, Saba F. Elhag, Ajaz A. Bhat, Waleed Aamer, Aljazi Al-Maraghi, Hala Alhaboub, Dalya Abuthaher, Ammira S. Al-Shabeeb Akil, Mohammad Haris, Khalid Fakhro,
and et al. 2025. "Functional Interpretation of a Novel Homozygous METTL5 Variant Associated with ADHD and Neurodevelopmental Abnormalities: A Case Report and Literature Review" Genes 16, no. 12: 1502.
https://doi.org/10.3390/genes16121502
APA Style
Hashem, S., Elhag, S. F., Bhat, A. A., Aamer, W., Al-Maraghi, A., Alhaboub, H., Abuthaher, D., Akil, A. S. A.-S., Haris, M., Fakhro, K., Nemer, G., & Kamal, M.
(2025). Functional Interpretation of a Novel Homozygous METTL5 Variant Associated with ADHD and Neurodevelopmental Abnormalities: A Case Report and Literature Review. Genes, 16(12), 1502.
https://doi.org/10.3390/genes16121502
