A case of a mild Wolfram Syndrome with concomitant ATP7B mutation.

R SquittiG CerchiaroI GiovannoniP FrancalanciM SiottoP MaffeiC RicordiM C Rongioletti

Published in: CellR4-- repair, replacement, regeneration, & reprogramming (2019)

This specific case report provides new insights into the potential interplay of ATP7B mutation in shaping a milder WS clinical picture.

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