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A Novel Mutation of the Vasopressin-Neurophysin II Gene in a Familial Neurohypophyseal Diabetes Insipidus.
Mi 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 Yoo
Endocrinol Metab. 2007;22(2):118-124.   Published online April 1, 2007
DOI: https://doi.org/10.3803/jkes.2007.22.2.118

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Progressive decline of vasopressin secretion in familial autosomal dominant neurohypophyseal diabetes insipidus presenting a novel mutation in the vasopressin-neurophysin II gene
Clinical Endocrinology. 2003;59(4):511-518   Crossref logo
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A Novel Mutation (R97C) in the Neurophysin Moiety of Prepro-Vasopressin-Neurophysin II Associated with Autosomal-Dominant Neurohypophyseal Diabetes Insipidus
Molecular Genetics and Metabolism. 1999;67(1):89-92   Crossref logo
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A novel mutation in the coding region for neurophysin-II is associated with autosomal dominant neurohypophyseal diabetes insipidus
Clinical Endocrinology. 1996;44(1):45-51   Crossref logo
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Clinical and molecular analysis of a Chinese family with autosomal dominant neurohypophyseal diabetes insipidus associated with a novel missense mutation in the vasopressin–neurophysin II gene
Endocrine. 2012;42(1):208-213   Crossref logo
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A Novel Mutation of the Vasopressin-Neurophysin II Gene in a Familial Neurohypophyseal Diabetes Insipidus
Journal of Korean Endocrine Society. 2007;22(2):118   Crossref logo
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A novel splice site mutation of the arginine vasopressin–neurophysin II gene identified in a kindred with autosomal dominant familial neurohypophyseal diabetes insipidus
Molecular Genetics and Metabolism. 2005;86(1-2):307-313   Crossref logo
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A New Missense Mutation of the Vasopressin-Neurophysin II Gene in a Family with Neurohypophyseal Diabetes insipidus
Hormone Research in Paediatrics. 2003;60(3):143-147   Crossref logo
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A missense mutation in the arginine-vasopressin neurophysin-II gene causes autosomal dominant neurohypophyseal diabetes insipidus in a Chinese family
Clinical Endocrinology. 2013;78(6):920-925   Crossref logo
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A Novel Arginine Vasopressin-Neurophysin II Mutation Causes Autosomal Dominant Neurohypophyseal Diabetes insipidus and Morphologic Pituitary Changes
Hormone Research in Paediatrics. 2000;53(5):239-245   Crossref logo
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Late-onset familial neurohypophyseal diabetes insipidus due to a novel mutation in the AVP gene
Clinical Endocrinology. 2012;77(4):586-592   Crossref logo
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