Male mice with deleted Wolframin (Wfs1) gene have reduced fertility

BACKGROUND: Wolfram Syndrome (WS) is an autosomal recessive disorder characterised by non-autoimmune diabetes mellitus, optic atrophy, cranial diabetes insipidus and sensorineural deafness. Some reports have described hypogonadism in male WS patients. The aim of our study was to find out whether Wfs...

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Detalles Bibliográficos
Autores principales: Noormets, Klari, Kõks, Sulev, Kavak, Ants, Arend, Andres, Aunapuu, Marina, Keldrimaa, Aivi, Vasar, Eero, Tillmann, Vallo
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2734842/
https://www.ncbi.nlm.nih.gov/pubmed/19664290
http://dx.doi.org/10.1186/1477-7827-7-82

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2734842/
https://www.ncbi.nlm.nih.gov/pubmed/19664290
http://dx.doi.org/10.1186/1477-7827-7-82

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