Latypov A.Sh., Proskurin E.V., Sidorova O.P., Vasilenko I.A., Kassina D.V., Bunak M.S. Intellectual development disorder syndrome with congenital anomalies of type 99, faceted female (OMIM: 300968), updated mutation in the USP9X gene. Russian Journal of Child Neurology. 2024;19(4):52-57. (In Russ.) https://doi.org/10.17650/2073-8803-2024-19-4-52-57
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