PublisherDOIYearVolumeIssuePageTitleAuthor(s)Link
Clinical Endocrinology10.1046/j.1365-2265.2003.01834.x2003594511-518Progressive decline of vasopressin secretion in familial autosomal dominant neurohypophyseal diabetes insipidus presenting a novel mutation in the vasopressin-neurophysin II genePaula C. L. Elias, Lucila L. K. Elias, Natalia Torres, Ayrton C. Moreira, Jose Antunes-Rodrigues, Margaret Castrohttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1046%2Fj.1365-2265.2003.01834.x, https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1046%2Fj.1365-2265.2003.01834.x, http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2265.2003.01834.x/fullpdf
Molecular Genetics and Metabolism10.1006/mgme.1999.2825199967189-92A Novel Mutation (R97C) in the Neurophysin Moiety of Prepro-Vasopressin-Neurophysin II Associated with Autosomal-Dominant Neurohypophyseal Diabetes InsipidusJonas Rutishauser, Peter Kopp, Mary Beth Gaskill, Thomas J. Kotlar, Gary L. Robertsonhttps://api.elsevier.com/content/article/PII:S1096719299928251?httpAccept=text/xml, https://api.elsevier.com/content/article/PII:S1096719299928251?httpAccept=text/plain
Journal of Korean Endocrine Society10.3803/jkes.2007.22.2.1182007222118A Novel Mutation of the Vasopressin-Neurophysin II Gene in a Familial Neurohypophyseal Diabetes InsipidusMi Jung Kim, Byung Wan Lee, In Kyung Jeong, Jun Goo Kang, Seong Jin Lee, Eun Gyung Hong, Hyeon Kyu Kim, Doo Man Kim, Jae Myung Yoo, Sung Hee Ihm, Moon Gi Choi, Hyung Joon Yoohttps://synapse.koreamed.org/DOIx.php?id=10.3803/jkes.2007.22.2.118, https://synapse.koreamed.org/pdf/10.3803/jkes.2007.22.2.118, http://synapse.koreamed.org/DOIx.php?id=10.3803/jkes.2007.22.2.118
Hormone Research in Paediatrics10.1159/0000725262003603143-147A New Missense Mutation of the Vasopressin-Neurophysin II Gene in a Family with Neurohypophyseal Diabetes insipidusM.T.F. Wolf, J. Dötsch, M. Metzler, M. Holder, R. Repp, W. Rascherhttps://www.karger.com/Article/Pdf/72526, https://www.karger.com/Article/Pdf/72526
Clinical Endocrinology10.1111/cen.121292013786920-925A missense mutation in the arginine-vasopressin neurophysin-II gene causes autosomal dominant neurohypophyseal diabetes insipidus in a Chinese familyDan Ye, FengQin Dong, WeiQin Lu, Zhe Zhang, XunLiang Lu, ChengJiang Li, YanNing Liuhttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fcen.12129, http://onlinelibrary.wiley.com/wol1/doi/10.1111/cen.12129/fullpdf
Endocrine10.1007/s12020-012-9606-22012421208-213Clinical and molecular analysis of a Chinese family with autosomal dominant neurohypophyseal diabetes insipidus associated with a novel missense mutation in the vasopressin–neurophysin II geneYongfeng Luo, Binbin Wang, Yu Qiu, Chuan Zhang, Chengluo Jin, Yakun Zhao, Qingguo Zhu, Xu Mahttp://link.springer.com/content/pdf/10.1007/s12020-012-9606-2.pdf, http://link.springer.com/article/10.1007/s12020-012-9606-2/fulltext.html, http://link.springer.com/content/pdf/10.1007/s12020-012-9606-2
The EMBO Journal10.1002/j.1460-2075.1992.tb05022.x199211119-23A missense mutation in the vasopressin-neurophysin precursor gene cosegregates with human autosomal dominant neurohypophyseal diabetes insipidus.U. Bahnsen, P. Oosting, D.F. Swaab, P. Nahke, D. Richter, H. Schmalehttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fj.1460-2075.1992.tb05022.x, http://onlinelibrary.wiley.com/wol1/doi/10.1002/j.1460-2075.1992.tb05022.x/fullpdf
Molecular Genetics and Metabolism10.1016/j.ymgme.2005.05.0092005861-2307-313A novel splice site mutation of the arginine vasopressin–neurophysin II gene identified in a kindred with autosomal dominant familial neurohypophyseal diabetes insipidusHyun-Jung Tae, Ki-Hyun Baek, Sun-Mi Shim, Soon-Jib Yoo, Moo-Il Kang, Bong-Yun Cha, Kwang-Woo Lee, Ho-Young Son, Sung-Koo Kanghttps://api.elsevier.com/content/article/PII:S109671920500171X?httpAccept=text/xml, https://api.elsevier.com/content/article/PII:S109671920500171X?httpAccept=text/plain
Hormone Research in Paediatrics10.1159/0000235732000535239-245A Novel Arginine Vasopressin-Neurophysin II Mutation Causes Autosomal Dominant Neurohypophyseal Diabetes insipidus and Morphologic Pituitary ChangesNicos Skordis, Philippos C. Patsalis, Joe A. Hettinger, Maria Kontou, Eleni Herakleous, M.R.S. Krishnamani, J.A. Phillips IIIhttps://www.karger.com/Article/Pdf/23573, https://www.karger.com/Article/Pdf/23573
Clinical Chemistry10.1093/clinchem/46.10.1699200046101699-1702Identification of Two Distinct Mutations at the Same Nucleotide Position, Concomitantly with a Novel Polymorphism in the Vasopressin-Neurophysin II Gene (AVP-NP II) in Two Dutch Families with Familial Neurohypophyseal Diabetes InsipidusAndré P Abbes, Bennie Bruggeman, Erica L T van den Akker, Marco R de Groot, Anton A M Franken, Valentijn R Drexhage, Henk Engelhttp://academic.oup.com/clinchem/article-pdf/46/10/1699/32729531/clinchem1699.pdf, http://academic.oup.com/clinchem/article-pdf/46/10/1699/32729531/clinchem1699.pdf