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2. Alhamoudi, Kheloud M, Bhat, Javaid, Nashabat, Marwan, Umair, Muhammad, Alfadhel, Majid. 2020. A Missense Mutation in the UGDH Gene Is Associated With Developmental Delay and Axial Hypotonia. In Frontiers in pediatrics, 8, 71. doi:10.3389/fped.2020.00071. https://pubmed.ncbi.nlm.nih.gov/32175296/
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7. Struck, Ann-Kathrin, Braun, Marina, Detering, Kim Aline, Metzger, Julia, Distl, Ottmar. 2020. A structural UGDH variant associated with standard Munchkin cats. In BMC genetics, 21, 67. doi:10.1186/s12863-020-00875-x. https://pubmed.ncbi.nlm.nih.gov/32605545/
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