Novel mutation of MAP3K1 gene in 46,XY DSD with complete gonadal dysgenesis
Objective: Swyer syndrome, or 46, XY complete gonadal dysgenesis, is a disorder of human sexual development which present with female external genitalia, lack of female reproductive organs, and a 46, XY karyotype. Many genes that participate in human sexual development have been implicated in the pa...
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| Autori principali: | , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Elsevier
2022-09-01
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| Serie: | Taiwanese Journal of Obstetrics & Gynecology |
| Soggetti: | |
| Accesso online: | http://www.sciencedirect.com/science/article/pii/S1028455922002297 |
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