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Oxford University Press

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Somatic Mutations Are Frequent and Increase with Age in Human Kidney Epithelial Cells

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Variable Somatic TIE2 Mutations in Half of Sporadic Venous Malformations

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KVLQT1 Mutations in Three Families with Familial or Sporadic Long QT Syndrome

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Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease

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