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A novel mutation Thr162Arg of the melanocortin 4 receptor gene in a Spanish children and adolescent population

✍ Scribed by M. C. Ochoa; C. Azcona; H. Biebermann; H. Brumm; C. Razquin; A.-K. Wermter; J. A. Martínez; J. Hebebrand; A. Hinney; M. J. Moreno-Aliaga; A. Marti; Grupo de Estudio Navarro de la Obesidad Infantil (GENOI) members


Book ID
108703677
Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
262 KB
Volume
66
Category
Article
ISSN
0300-0664

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The melanocortin 1 receptor (MC1R) gene is a major determinant of human pigmentation and specific allelic variants have been associated with red hair and sun sensitive skin types as well as increased skin cancer risk in Caucasian individuals. We screened for allelic variants the entire MC1R coding r