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AVPR2 gene

Discuss publications and research concerning the AVPR2 gene.

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Related literature

SyMetrics: an integrated machine learning model for evaluating the pathogenicity of synonymous variants in the human genome.
AVPR2
The natural history of untreated X-linked nephrogenic diabetes insipidus with mutation in the vasopressin V2 receptor gene.
AVPR2
Hereditary Nephrogenic Diabetes Insipidus: Pathophysiology and Possible Treatment. An Update.
AVPR2
[Nephrogenic syndrome of inappropriate antidiuresis: Early diagnosis avoids severe hyponatremia complications].
AVPR2
Nephrogenic syndrome of inappropriate antidiuresis secondary to an activating mutation in the arginine vasopressin receptor AVPR2.
AVPR2
Genetic forms of nephrogenic diabetes insipidus (NDI): Vasopressin receptor defect (X-linked) and aquaporin defect (autosomal recessive and dominant).
AVPR2
Genetic analysis of a congenital nephrogenic diabetes insipidus pedigree.
AVPR2
Nephrogenic diabetes insipidus: essential insights into the molecular background and potential therapies for treatment.
AVPR2
Functional polymorphisms affecting the clinically important arginine-137 residue of AVPR2 do not influence serum sodium concentration at the population level.
AVPR2
Congenital nephrogenic diabetes insipidus: the current state of affairs.
AVPR2

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