Publications
Acta diabetologicaMar 2023 DOI:
10.1007/s00592-023-02065-4

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

Silvestri, Francesca; Tromba, Valeria; Schiaffini, Riccardo; Costantino, Francesco; Barbetti, Fabrizio; Prudente, Sabrina
Product Used
NGS
Product Used
NGS

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