Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel missense mutation in AVP gene in a large Italian kindred.
Carlotta MarzocchiSilvia CantaraAlfonso SagnellaMaria Grazia CastagnaMarco CapezzonePublished in: Endocrine (2021)
This is the first study that identified a novel missense p.C52S mutation as causative of central diabetes insipidus in a large Italian pedigree.