Consider CUX1 variants in children with a variation of sex development: a case report and review of the literature

Abstract Background The Cut Homeobox 1 (CUX1) gene has been implicated in a number of developmental processes and has recently emerged as an important cause of developmental delay and impaired intellectual development. Individuals with variants in CUX1 have been described with a variety of co-morbid...

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Hlavní autoři: Lynn Tan (Autor), Shelley G. Young (Autor), Andrew H. Sinclair (Autor), Matthew F. Hunter (Autor), Katie L. Ayers (Autor)
Médium: Kniha
Vydáno: BMC, 2024-08-01T00:00:00Z.
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