Familial neurohypophyseal diabetes insipidus in 13 kindreds and 2 novel mutations in the vasopressin gene
- Patti, Giuseppa
- Scianguetta, Saverio
- Roberti, Domenico
- Di Mascio, Alberto
- Balsamo, Antonio
- Brugnara, Milena
- Cappa, Marco
- Casale, Maddalena
- Cavarzere, Paolo
- Cipriani, Sarah
- Corbetta, Sabrina
- Gaudino, Rossella
- Iughetti, Lorenzo
- Martini, Lucia
- Napoli, Flavia
- Peri, Alessandro
- Salerno, Mariacarolina
- Salerno, Roberto
- Passeri, Elena
- Maghnie, Mohamad
- Perrotta, Silverio
- Di Iorgi, Natascia.
DOIAbstract
Autosomal dominant neurohypophyseal diabetes insipidus (adNDI) is caused by arginine vasopressin (AVP) deficiency resulting from mutations in the AVP-NPII gene encoding the AVP preprohormone
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