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Publikováno v:
Frontiers in Molecular Neuroscience, Vol 8 (2015)
BackgroundMutations in WFS1 gene cause Wolfram syndrome, which is a rare autosomal recessive disorder, characterized by diabetes insipidus, diabetes mellitus, optic nerve atrophy and deafness (DIDMOAD). The WFS1 gene product wolframin is located in t
Externí odkaz:
https://doaj.org/article/005f5a76ba1544b8afc1c65ecb99b60b
