9402099

Source:http://linkedlifedata.com/resource/pubmed/id/9402099

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0677501
pubmed:issue	12
pubmed:dateCreated	1998-2-13
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9013836
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/AQP2 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Aquaporin 2, http://linkedlifedata.com/resource/pubmed/chemical/Aquaporin 6, http://linkedlifedata.com/resource/pubmed/chemical/Aquaporins, http://linkedlifedata.com/resource/pubmed/chemical/Arginine Vasopressin, http://linkedlifedata.com/resource/pubmed/chemical/Deamino Arginine Vasopressin, http://linkedlifedata.com/resource/pubmed/chemical/Ion Channels, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Vasopressin
pubmed:status	MEDLINE
pubmed:month	Dec
pubmed:issn	1046-6673
pubmed:author	pubmed-author:BichetD GDG, pubmed-author:OkscheAA, pubmed-author:RosenthalWW
pubmed:issnType	Print
pubmed:volume	8
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1951-8
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:9402099-Amino Acid Sequence, pubmed-meshheading:9402099-Aquaporin 2, pubmed-meshheading:9402099-Aquaporin 6, pubmed-meshheading:9402099-Aquaporins, pubmed-meshheading:9402099-Arginine Vasopressin, pubmed-meshheading:9402099-Deamino Arginine Vasopressin, pubmed-meshheading:9402099-Dehydration, pubmed-meshheading:9402099-Diabetes Insipidus, Nephrogenic, pubmed-meshheading:9402099-Drug Resistance, pubmed-meshheading:9402099-Female, pubmed-meshheading:9402099-Founder Effect, pubmed-meshheading:9402099-Genetic Heterogeneity, pubmed-meshheading:9402099-Heterozygote Detection, pubmed-meshheading:9402099-History, 17th Century, pubmed-meshheading:9402099-History, 18th Century, pubmed-meshheading:9402099-Humans, pubmed-meshheading:9402099-Incidence, pubmed-meshheading:9402099-Infant, pubmed-meshheading:9402099-Infant, Newborn, pubmed-meshheading:9402099-Intellectual Disability, pubmed-meshheading:9402099-Ion Channels, pubmed-meshheading:9402099-Ireland, pubmed-meshheading:9402099-Kidney Failure, Chronic, pubmed-meshheading:9402099-Male, pubmed-meshheading:9402099-Models, Biological, pubmed-meshheading:9402099-Models, Molecular, pubmed-meshheading:9402099-Molecular Sequence Data, pubmed-meshheading:9402099-Mutation, pubmed-meshheading:9402099-Nephrons, pubmed-meshheading:9402099-Nova Scotia, pubmed-meshheading:9402099-Prenatal Diagnosis, pubmed-meshheading:9402099-Prevalence, pubmed-meshheading:9402099-Protein Conformation, pubmed-meshheading:9402099-Receptors, Vasopressin, pubmed-meshheading:9402099-X Chromosome
pubmed:year	1997
pubmed:articleTitle	Congenital nephrogenic diabetes insipidus.
pubmed:affiliation	Department of Medicine, Université de Montréal and Research Centre, Hôpital du Sacré-Coeur de Montréal, Quebec, Canada.
pubmed:publicationType	Journal Article, Review, Historical Article, Research Support, Non-U.S. Gov't