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A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome. | Barrientos, A; Volpini, V; Casademont, J; GenÃs, D; Manzanares, J M; Ferrer, I; Corral, J; Cardellach, F; Urbano-Márquez, A; Estivill, X; Nunes, V; | |
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