[Retracted] A Novel Missense Mutation of Arginine Vasopressin Receptor 2 in a Chinese Family with Congenital Nephrogenic Diabetes Insipidus: X-Chromosome Inactivation in Female CNDI Patients with Heterozygote 814A>G Mutation

<div>The imaging feature of the proband. (a) Pituitary MRI showed normal anterior and posterior pituitary. (b) Urinary system CT scan showed bilateral ureterectasis and hydronephrosis combined with right kidney atrophy.</div>

BioMed Research International

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Figure 2

Figure 2: [Retracted] A Novel Missense Mutation of Arginine Vasopressin Receptor 2 in a Chinese Family with Congenital Nephrogenic Diabetes Insipidus: X-Chromosome Inactivation in Female CNDI Patients with Heterozygote 814A>G Mutation 

Figure 2 | [Retracted] A Novel Missense Mutation of Arginine Vasopressin Receptor 2 in a Chinese Family with Congenital Nephrogenic Diabetes Insipidus: X-Chromosome Inactivation in Female CNDI Patients with Heterozygote 814A>G Mutation 