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rdf:type |
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lifeskim:mentions |
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pubmed:dateCreated |
2010-4-1
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pubmed:abstractText |
Insulin gene (INS) mutations have recently been described as a common cause of permanent neonatal diabetes (PNDM) and a rare cause of diabetes diagnosed in childhood or adulthood.
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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:issn |
1471-2350
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pubmed:author |
pubmed-author:AnderssonEhm AEA,
pubmed-author:BarbettiFabrizioF,
pubmed-author:BergholdtRegineR,
pubmed-author:BoesgaardTrine WTW,
pubmed-author:CinekOndrejO,
pubmed-author:DammPeterP,
pubmed-author:HansenTorbenT,
pubmed-author:LakeR IRI,
pubmed-author:LauenborgJeannetJ,
pubmed-author:ObermannovaBarboraB,
pubmed-author:PedersenOlufO,
pubmed-author:PisingerCharlottaC,
pubmed-author:PociotFlemmingF,
pubmed-author:PruhovaStepankaS
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pubmed:issnType |
Electronic
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pubmed:volume |
11
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
42
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:20226046-Diabetes, Gestational,
pubmed-meshheading:20226046-Diabetes Mellitus, Type 1,
pubmed-meshheading:20226046-Diabetes Mellitus, Type 2,
pubmed-meshheading:20226046-Female,
pubmed-meshheading:20226046-Genetic Variation,
pubmed-meshheading:20226046-Humans,
pubmed-meshheading:20226046-Insulin,
pubmed-meshheading:20226046-Male,
pubmed-meshheading:20226046-Mutation,
pubmed-meshheading:20226046-Pedigree,
pubmed-meshheading:20226046-Phenotype,
pubmed-meshheading:20226046-Pregnancy,
pubmed-meshheading:20226046-Young Adult
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pubmed:year |
2010
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pubmed:articleTitle |
Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY).
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pubmed:affiliation |
Steno Diabetes Centre and Hagedorn Research Institute, Gentofte, Denmark. tweb@hagedorn.dk
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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