Cargando…
The DAX1 mutation in a patient with hypogonadotropic hypogonadism and adrenal hypoplasia congenita causes functional disruption of induction of spermatogenesis
Autores principales: | Ponikwicka-Tyszko, Donata, Kotula-Balak, Malgorzata, Jarzabek, Katarzyna, Bilinska, Barbara, Wolczynski, Slawomir |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3430789/ https://www.ncbi.nlm.nih.gov/pubmed/22562240 http://dx.doi.org/10.1007/s10815-012-9778-y |
Ejemplares similares
-
Delayed-onset adrenal hypoplasia congenita and hypogonadotropic
hypogonadism caused by a novel mutation in DAX1
por: Liu, Siyue, et al.
Publicado: (2019) -
Adrenal Hypoplasia Congenita: A Rare Cause of Primary Adrenal Insufficiency and Hypogonadotropic Hypogonadism
por: Loureiro, Marta, et al.
Publicado: (2015) -
Birth after TESE–ICSI in a man with hypogonadotropic hypogonadism and congenital adrenal hypoplasia linked to a DAX-1 (NR0B1) mutation
por: Frapsauce, C., et al.
Publicado: (2011) -
Induction of spermatogenesis in men with hypogonadotropic hypogonadism
por: Morris, Guy C., et al.
Publicado: (2021) -
Identification and Functional Analysis of Six DAX1 Mutations in Patients With X-Linked Adrenal Hypoplasia Congenita
por: Suthiworachai, Chanisara, et al.
Publicado: (2018)