Alhamoudi, K. M., Bhat, J., Nashabat, M., Alharbi, M., Alyafee, Y., Asiri, A., . . . Alfadhel, M. (2020). A Missense Mutation in the UGDH Gene Is Associated With Developmental Delay and Axial Hypotonia. Front Pediatr.
Style de citation ChicagoAlhamoudi, Kheloud M., Javaid Bhat, Marwan Nashabat, Masheal Alharbi, Yusra Alyafee, Abdulaziz Asiri, Muhammad Umair, et Majid Alfadhel. "A Missense Mutation in the UGDH Gene Is Associated With Developmental Delay and Axial Hypotonia." Front Pediatr 2020.
Style de citation MLAAlhamoudi, Kheloud M., et al. "A Missense Mutation in the UGDH Gene Is Associated With Developmental Delay and Axial Hypotonia." Front Pediatr 2020.
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