Two novel AMHR2 gene variants in monozygotic twins with persistent Müllerian duct syndrome: A case report and functional study

BACKGROUND: Persistent Müllerian duct syndrome (PMDS) is an autosomal recessive congenital abnormality in which Müllerian derivatives, uterus, cervix, upper two‐thirds of the vagina, and fallopian tubes persist in otherwise normally virilized males. Mutations in anti‐Müllerian hormone (AMH) and AMH...

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Detalles Bibliográficos
Autores principales: Chen, Hong, Lin, Peng, Yuan, Xin, Chen, Ruimin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9356563/
https://www.ncbi.nlm.nih.gov/pubmed/35655435
http://dx.doi.org/10.1002/mgg3.1999

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9356563/
https://www.ncbi.nlm.nih.gov/pubmed/35655435
http://dx.doi.org/10.1002/mgg3.1999

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