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Lack of red hair phenotype in a North‐African obese child homozygous for a novel POMC null mutation: nonsense‐mediated decay RNA evaluation and hair pigment chemical analysis
Author(s) -
Cirillo G.,
Marini R.,
Ito S.,
Wakamatsu K.,
Scianguetta S.,
Bizzarri C.,
Romano A.,
Grandone A.,
Perrone L.,
Cappa M.,
Miraglia del Giudice E.
Publication year - 2012
Publication title -
british journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.304
H-Index - 179
eISSN - 1365-2133
pISSN - 0007-0963
DOI - 10.1111/j.1365-2133.2012.11060.x
Subject(s) - proopiomelanocortin , melanocortin 1 receptor , melanocortin , adrenocorticotropic hormone , coat , biology , endocrinology , melanocyte stimulating hormone , medicine , hair follicle , phenotype , melanocortin 3 receptor , melanin , receptor , hypothalamus , microbiology and biotechnology , gene , hormone , melanocortin receptor , genetics , paleontology
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