A single base substitution in the coding region for neurophysin II associated with familial central diabetes insipidus.

Lignende værker

• SAT-093 Two Cases of Autosomal Dominant Familial Central Diabetes Insipidus: A Novel Variant in Neurophysin II Region of AVP Gene
  af: Ramirez, Biochemist, Pablo, et al.
  Udgivet: (2020)
• Possible involvement of inefficient cleavage of preprovasopressin by signal peptidase as a cause for familial central diabetes insipidus.
  af: Ito, M, et al.
  Udgivet: (1993)
• Identification of 13 new mutations in the vasopressin-neurophysin II gene in 17 kindreds with familial autosomal dominant neurohypophyseal diabetes insipidus.
  af: Rittig, S., et al.
  Udgivet: (1996)
• Neurophysin biosynthesis in normal rats and in rats with hereditary diabetes insipidus.
  af: Brownstein, M J, et al.
  Udgivet: (1977)
• Central diabetes insipidus
  af: Arima, Hiroshi, et al.
  Udgivet: (2016)