![](/img/cover-not-exists.png)
Mutation update and uncommon phenotypes in a French cohort of 96 patients with WFS1 -related disorders
Chaussenot, A., Rouzier, C., Quere, M., Plutino, M., Ait-El-Mkadem, S., Bannwarth, S., Barth, M., Dollfus, H., Charles, P., Nicolino, M., Chabrol, B., Vialettes, B., Paquis-Flucklinger, V.Volume:
87
Language:
english
Journal:
Clinical Genetics
DOI:
10.1111/cge.12437
Date:
May, 2015
File:
PDF, 787 KB
english, 2015