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doi: 10.2337/db12-0466

The most commonly mutated genes are the potassium inwardly-rectifying channel, subfamily J, member 11 (KCNJ11), ATP-binding cassette transporter, subfamily C, member 8 (ABCC8), and insulin (INS) genes
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Se confermata la carenza di carnitina, possono essere prescritti integratori di carnitina per correggere il problema, ma sempre importante seguire le indicazioni del medico e non auto-prescriversi integratori senza supervisione
