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Prohormone convertase 2 activity is increased in the hippocampus of Wfs1 knockout mice
Background: Mutations in WFS1 gene cause Wolfram syndrome, which is a rare autosomal recessive disorder, characterized by diabetes insipidus, diabetes mellitus, optic nerve atrophy, and deafness. The WFS1 gene product wolframin is located in the endoplasmic reticulum. Mice lacking this gene exhibit...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Front Mol Neurosci |
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| Κύριοι συγγραφείς: | , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Frontiers Media S.A.
2015
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4548212/ https://ncbi.nlm.nih.gov/pubmed/26379490 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnmol.2015.00045 |
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