Heterozygous versus homozygous phenotype caused by the same MC4R mutation: novel mutation affecting a large consanguineous kindred

Abstract Background The hypothalamic G-protein-coupled-receptor melanocortin-4 receptor (MC4R) is a key player in the central circuit regulating energy expenditure and appetite. Heterozygous loss-of-function MC4R mutations are the most common known genetic cause of monogenic human obesity, with more...

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Bibliographic Details
Main Authors: Max Drabkin (Author), Ohad S. Birk (Author), Ruth Birk (Author)
Format: Book
Published: BMC, 2018-08-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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