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FU was partly supported by grants from the NIH/NIDDK (DK132090, DK020579) and the NIH/National Center for Advancing Translational Sciences (NCATS) (TR002065, TR000448) and philanthropic support from the Silberman Fund, the Ellie White Foundation for Rare Genetic Disorders, the Snow Foundation, the Unravel Wolfram Syndrome Fund, the Stowe Fund, the Feiock Fund, the Cachia Fund, the Gildenhorn Fund, the Eye Hope Foundation, Ontario Wolfram League, Associazione GentianSindrome di Wolfram Italia, Alianza de Familias Afectadas por el Sindrome Wolfram Spain, Wolfram Syndrome UK and the Association Syndrome de Wolfram France

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PMID 14554208