Nephrogenic Diabetes Insipidus
Last Posted: May 27, 2021
- Integrating Population Variants and Protein Structural Analysis to Improve Clinical Genetic Diagnosis and Treatment in Nephrogenic Diabetes Insipidus.
Liao Panli et al. Frontiers in pediatrics 2021 9566524
- Genetic forms of nephrogenic diabetes insipidus (NDI): Vasopressin receptor defect (X-linked) and aquaporin defect (autosomal recessive and dominant).
Bichet Daniel G, et al. Best practice & research. Clinical endocrinology & metabolism 2016 3 (2) 263-76
- Nephrogenic diabetes insipidus
From NCATS Genetic and Rare Diseases Information Center
- Correlation between AVPR2 mutations and urinary AQP2 excretion in patients with nephrogenic diabetes insipidus.
Kotnik Primoz, et al. Journal of pediatric endocrinology & metabolism : JPEM 2007 4 (4) 483-9
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