Cataract as a Phenotypic Marker for a Mutation in WFS1, the Wolfram Syndrome Gene
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G. Rondouin | P. Amati‐Bonneau | G. Lenaers | P. Reynier | C. Hamel | C. Blanchet | I. Meunier | S. Lopez | V. Paquis-Flucklinger | Salah Mohamed Cherif Titah