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13816810.2012.755631
13816810.2012.755631
http://dx.doi.org/10.3109/13816810.2012.755631
Expansion of the clinical ocular spectrum of Wolfram Syndrome in a family carrying a novel WFS1 gene deletion.
P356
Q54273588-D76E575F-9CB9-41BB-8480-68B9E837C4C6
P356
13816810.2012.755631
http://dx.doi.org/10.3109/13816810.2012.755631