Identification of AMH and AMHR2 Variants Led to the Diagnosis of Persistent Müllerian Duct Syndrome in Three Cases

Persistent Müllerian duct syndrome (PMDS) is a rare autosomal recessive disorder of sexual development in males, defined by the presence of Müllerian remnants with otherwise normal sexual differentiation. Mutations in anti-Müllerian hormone (AMH) and AMH receptor type 2 (AMHR2) genes are the main ca...

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Detalles Bibliográficos
Autores principales: Liu, Yang, Wang, Sida, Lan, Ruzhu, Yang, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8774887/
https://www.ncbi.nlm.nih.gov/pubmed/35052499
http://dx.doi.org/10.3390/genes13010159

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8774887/
https://www.ncbi.nlm.nih.gov/pubmed/35052499
http://dx.doi.org/10.3390/genes13010159

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