Mutation Screening of the Urocortin Gene: Identification of New Single Nucleotide Polymorphisms and Association Studies with Obesity in French Caucasians - Delplanque, J.; Vasseur, F.; Durand, E.; Abderrahmani, A.; Dina, C.; Waeber, G.; Guy-Grand, B.; Clement, K.; Weill, J.; Boutin, P.; Froguel, P. (The journal of clinical endocrinology and metabolism, 2002)
Keywords: 3' Untranslated regions; Adult; Aged; Base Sequence - genetics; Biological and medical sciences; Body mass index; Chromosome 2; Chromosomes, Human, Pair 2 - genetics; Corticotropin-Releasing Hormone - genetics; Diabetes mellitus; Endocrinopathies; Female; France; Gene Frequency; Gene mapping; General aspects. Associated endocrine diseases. Endocrine paraneoplasic syndromes; Genetic analysis; Genetic diversity; Genetic Testing; Genetics; Human genetics; Humans; Leptin; Life Sciences; Male; Medical sciences; Metabolic diseases; Middle Aged; Mutation; Obesity; Obesity - genetics; Peptide mapping; Phenotypes; Phenotypic variations; Polymorphism, Genetic - genetics; Quantitative Trait, Heritable; Single-nucleotide polymorphism; Urocortin; Urocortins; White people; White People - genetics; France; Obesity; Linkage; Nutrition disorder; Identification; Medical screening; Protein; Body mass index; Urocortin; Phenotype; Nucleotide; Candidate gene; Mutation; Caucasoid; Locus; Nutritional status; Polymorphism