APA (7th ed.) Citation

Kheloud M. Alhamoudi, Javaid Bhat, Marwan Nashabat, Masheal Alharbi, Yusra Alyafee, Abdulaziz Asiri, . . . Majid Alfadhel. (2020). A Missense Mutation in the UGDH Gene Is Associated With Developmental Delay and Axial Hypotonia. Frontiers Media S.A..

Chicago Style (17th ed.) Citation

Kheloud M. Alhamoudi, Javaid Bhat, Marwan Nashabat, Masheal Alharbi, Yusra Alyafee, Abdulaziz Asiri, Muhammad Umair, Majid Alfadhel, and Majid Alfadhel. A Missense Mutation in the UGDH Gene Is Associated With Developmental Delay and Axial Hypotonia. Frontiers Media S.A., 2020.

MLA (9th ed.) Citation

Kheloud M. Alhamoudi, et al. A Missense Mutation in the UGDH Gene Is Associated With Developmental Delay and Axial Hypotonia. Frontiers Media S.A., 2020.

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