Mutation update and uncommon phenotypes in a French cohort of 96 patients with WFS1‐related disorders

Publisher: John Wiley & Sons Inc

E-ISSN: 1399-0004|87|5|430-439

ISSN: 0009-9163

Source: CLINICAL GENETICS, Vol.87, Iss.5, 2015-05, pp. : 430-439

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Abstract