Associated Papers
Genetic variations of type 2 and type 3 von Willebrand diseases in Thailand.
Lauhasurayotin S et al.
Journal of Clinical Pathology, 2024
Familial neurohypophyseal diabetes insipidus: clinical, genetic and functional studies of novel mutations in the arginine vasopressin gene.
Alvelos MI et al.
Pituitary, 2021
Central Diabetes Insipidus Caused by Arginine Vasopressin Gene Mutation: Report of a Novel Mutation and Review of Literature.
Feldkamp LLI et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme, 2020
Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel nonsense mutation in AVP-NPII gene.
Yang H et al.
Experimental and Therapeutic Medicine, 2019
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