A case of a mild Wolfram Syndrome with concomitant <i>ATP7B</i> mutation.

Squitti, R; Cerchiaro, G; Giovannoni, I; Francalanci, P; Siotto, M; Maffei, P; Ricordi, C; Rongioletti, M C

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

Squitti, R; Cerchiaro, G; Giovannoni, I; Francalanci, P; Siotto, M; Maffei, P; Ricordi, C; Rongioletti, M C.

Afiliación

Squitti R; IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli, Brescia, Italy.
Cerchiaro G; Center of Natural Sciences and Humanities, Federal University of ABC - UFABC, Santo André, São Paulo, Brazil.
Giovannoni I; Department of Pathology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Francalanci P; Department of Pathology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Siotto M; IRCCS Fondazione Don Carlo Gnocchi, Milan, Italy.
Maffei P; Department of Medicine (DIMED), Clinica Medica 3, Padua University Hospital, Italy.
Ricordi C; Diabetes Research Institute and Cell Transplant Center, University of Miami, Miami, FL, USA.
Rongioletti MC; Department of Laboratory Medicine, Research and Development Division, 'San Giovanni Calibita', Fatebenefratelli Hospital, Isola Tiberina, Rome, Italy.

CellR4 Repair Replace Regen Reprogram ; 72019.

Article en En | MEDLINE | ID: mdl-33869661

Palabras clave

ATP7B; Copper; Diabetes; Wolfram Syndrome

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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: CellR4 Repair Replace Regen Reprogram Año: 2019 Tipo del documento: Article País de afiliación: Italia

Texto completo

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PubMed Links

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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: CellR4 Repair Replace Regen Reprogram Año: 2019 Tipo del documento: Article País de afiliación: Italia