Source:http://linkedlifedata.com/resource/pubmed/id/19170714
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
5
|
| pubmed:dateCreated |
2009-10-8
|
| pubmed:abstractText |
Mutations in the insulin receptor (IR) gene are known to cause severe insulin resistance. Although clinical features due to a mutation can be diverse, hypoglycaemia is found in some cases. A family with a female proband diagnosed with type A insulin resistance syndrome was studied. Clinical characteristics were compared with the Arginine1174Glutamine (R1174N) mutation reported in the literature.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Nov
|
| pubmed:issn |
1365-2265
|
| pubmed:author | |
| pubmed:issnType |
Electronic
|
| pubmed:volume |
71
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
659-65
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| pubmed:meshHeading |
pubmed-meshheading:19170714-Adolescent,
pubmed-meshheading:19170714-Adult,
pubmed-meshheading:19170714-Child,
pubmed-meshheading:19170714-Female,
pubmed-meshheading:19170714-Glucose Clamp Technique,
pubmed-meshheading:19170714-Glucose Tolerance Test,
pubmed-meshheading:19170714-Humans,
pubmed-meshheading:19170714-Hyperinsulinism,
pubmed-meshheading:19170714-Insulin Resistance,
pubmed-meshheading:19170714-Male,
pubmed-meshheading:19170714-Mutation, Missense,
pubmed-meshheading:19170714-Receptor, Insulin
|
| pubmed:year |
2009
|
| pubmed:articleTitle |
Hyperinsulinaemic hypoglycaemia associated with a heterozygous missense mutation of R1174W in the insulin receptor (IR) gene.
|
| pubmed:affiliation |
Department of Endocrinology and Diabetes Centre, The First Affiliated Hospital of Sun Yat-sen University, #58 Zhongshan Er Road, Guangzhou, Guangdong, P.R. China.
|
| pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|