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Type I hyperprolinemia and proline dehydrogenase (PRODH) mutations in four Italian children with epilepsy and mental retardation

Di Rosa, Gabriellaa; Pustorino, Giuseppinaa; Spano, Mariaa; Campion, Dominiqued; Calabrò, Marilenaa; Aguennouz, Mohammedb; Caccamo, Danielac; Legallic, Solennd; Sgro, Domenica Luciaa; Bonsignore, Mariaa; Tortorella, Gaetanoa

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doi: 10.1097/YPG.0b013e3282f08a3d
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© 2008 Wolters Kluwer Health | Lippincott Williams & Wilkins