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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 Capezzone
Published 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.
Keyphrases
  • type diabetes
  • cardiovascular disease
  • intellectual disability
  • copy number
  • genome wide
  • gene expression
  • autism spectrum disorder
  • dna methylation
  • skeletal muscle
  • genome wide identification