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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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| Päätekijät: | , , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2009
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2734842/ https://ncbi.nlm.nih.gov/pubmed/19664290 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1477-7827-7-82 |
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