rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
6
|
pubmed:dateCreated |
2009-6-10
|
pubmed:abstractText |
Mutations in the melanocortin 4 receptor ( MC4R) gene are the most frequent cause of monogenic forms of obesity, but the reported prevalences of mutations in obese individuals diverge, varying from 0.2 to 5.8%.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jun
|
pubmed:issn |
1439-3646
|
pubmed:author |
|
pubmed:issnType |
Electronic
|
pubmed:volume |
117
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
266-73
|
pubmed:meshHeading |
pubmed-meshheading:19301229-Adolescent,
pubmed-meshheading:19301229-Adult,
pubmed-meshheading:19301229-Aged,
pubmed-meshheading:19301229-Aged, 80 and over,
pubmed-meshheading:19301229-Amino Acid Substitution,
pubmed-meshheading:19301229-DNA Mutational Analysis,
pubmed-meshheading:19301229-Female,
pubmed-meshheading:19301229-Humans,
pubmed-meshheading:19301229-Male,
pubmed-meshheading:19301229-Mass Screening,
pubmed-meshheading:19301229-Middle Aged,
pubmed-meshheading:19301229-Mutation, Missense,
pubmed-meshheading:19301229-Norway,
pubmed-meshheading:19301229-Obesity,
pubmed-meshheading:19301229-Receptor, Melanocortin, Type 4
|
pubmed:year |
2009
|
pubmed:articleTitle |
Mutations in the melanocortin 4 receptor (MC4R) gene in obese patients in Norway.
|
pubmed:affiliation |
Department of Medical Genetics, Ullevål University Hospital, Oslo, Norway. teresia.wangensteen@medisin.uio.no
|
pubmed:publicationType |
Journal Article,
Clinical Trial,
Research Support, Non-U.S. Gov't,
Multicenter Study
|