Record #66278
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 814AG Mutation
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Original paper date
Jul 12, 2022
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Pre-retraction
1
Same day
1
Post-retraction
2
% post-retraction
50.0%
~0.6 citations/yr before retraction · ~0.8 citations/yr after
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