Early diagnosis of Werner’s syndrome using exome-wide sequencing in a single, atypical patient by Eleanor eRaffan, Liam A Hurst, Saeed eAl Turki, Gillian eCarpenter, Carol eScott, Allan eDaly, Alison eCoffey, Sanjeev eBhaskar, Eleanor eHoward, Naz eKhan, Helen eKingston, Aarno ePalotie, David Bousfield Savage, Mark eO'Driscoll, Claire eSmith, Stephen eO'Rahilly, Inês eBarroso, Inês eBarroso, Robert Kenneth Semple

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