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The Arg1379His mutation in ABCC8 causes monogenic diabetes with variable phenotype presentation and incomplete penetrance.

Acta diabetologica - 1 Jul 2023

Silvestri Francesca, Tromba Valeria, Schiaffini Riccardo, Costantino Francesco, Barbetti Fabrizio, Prudente Sabrina

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PMID: 36944758
DOI: 10.1007/s00592-023-02065-4

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