Mutational analysis of the pro-opiomelanocortin gene in French obese children led to the identification of a novel deleterious heterozygous mutation located in the alpha-melanocyte stimulating hormone domain.
published in: Pediatric Research
date of publication: 2008-02-01
language: English
main subject: obesity, mutational analysis
Cites articles 21
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Article - wd:Q46842631