Open Access[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
Author(s) -
Li Zang,
Yuping Gong,
Yijun Li,
Jingtao Dou,
Zhaohui Lyu,
Xiaoqing Su,
Yawei Zhang,
Yiming Mu
Publication year - 2022
Publication title -
biomed research international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.772
H-Index - 126
eISSN - 2314-6141
pISSN - 2314-6133
DOI - 10.1155/2022/7073158
Subject(s) - missense mutation , nephrogenic diabetes insipidus , arginine , diabetes insipidus , vasopressin , mutation , endocrinology , heterozygote advantage , medicine , genetics , biology , gene , allele , amino acid
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