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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
7
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pubmed:dateCreated |
2005-7-8
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pubmed:abstractText |
Autosomal dominant neurohypophyseal diabetes insipidus (ADNDI) has been known as a rare disorder transmitted as an autosomal dominant trait, characterized by polyuria and polydipsia, and caused by deficient neurosecretion of arginine vasopressin precursor (AVP-NPII). We reported an ADNDI family with linkage to chromosome 20p13 but without mutations in the AVP-NPII gene.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0021-972X
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
90
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4388-93
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:15811933-Adolescent,
pubmed-meshheading:15811933-Adult,
pubmed-meshheading:15811933-Chromosomes, Human, Pair 20,
pubmed-meshheading:15811933-Diabetes Insipidus, Neurogenic,
pubmed-meshheading:15811933-Genes, Dominant,
pubmed-meshheading:15811933-Genetic Linkage,
pubmed-meshheading:15811933-Haplotypes,
pubmed-meshheading:15811933-Humans,
pubmed-meshheading:15811933-Male,
pubmed-meshheading:15811933-Middle Aged,
pubmed-meshheading:15811933-Mutation,
pubmed-meshheading:15811933-Neurophysins,
pubmed-meshheading:15811933-Polymerase Chain Reaction,
pubmed-meshheading:15811933-Protein Precursors,
pubmed-meshheading:15811933-Vasopressins
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pubmed:year |
2005
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pubmed:articleTitle |
Autosomal dominant neurohypophyseal diabetes insipidus with linkage to chromosome 20p13 but without mutations in the AVP-NPII gene.
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pubmed:affiliation |
Shanghai Clinical Center for Endocrine and Metabolic Diseases, Shanghai Institute of Endocrine and Metabolic Diseases, Ruijin Hospital, Shanghai Second Medical University, Ruijin Er Lu, Shanghai 200025, People's Republic of China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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