The DAX1 mutation in a patient with hypogonadotropic hypogonadism and adrenal hypoplasia congenita causes functional disruption of induction of spermatogenesis

Detalles Bibliográficos
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:
Genetics
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

Internet

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

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